XomeDxSlice Tool

Now Available - NEW XomeDxSlice Xpanded – Custom slice testing with trio analysis for lists >150 genes.

INSTRUCTIONS (AND TIPS)

ENTER GENES BELOW AND CLICK "ADD GENES TO SLICE"

If cutting and pasting from another document, please be sure to list EITHER one gene symbol per line OR enter a comma-separated list.


OR

SEARCH BY GENE SYMBOL OR PHENOTYPE (HPO TERM)

You may also use this search to review average exome sequencing coverage by entering the gene symbol below.

SELECTED GENES FOR YOUR SLICE

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  SUGGESTED CUSTOM SLICES  

Customize below OR enter Suggested Slice ID on printed requisition form
(e.g. 706 XomeDxSlice - Slice ID: CS-Albinism).

Suggested Slice IDSuggested Gene List Name
CS-AlbinismAlbinism
CS-AlportAlport Syndrome
CS-AAAplastic Anemia
CS-AutoImmuneAutoimmune Disorders
CS-BBSBardet-Biedl Syndrome
CS-BMFBone Marrow Failure Syndromes
CS-CVIDCommon Variable Immune Deficiency
CS-CKUTCongenital Kidney and Urinary Tract (CKUT) Anomalies
CS-DSDDisorders of Sex Development
CS-EDEctodermal Dysplasia
CS-FAFanconi Anemia
CS-AnemiaHemolytic Anemia
CS-HeterotaxyHeterotaxy
CS-IBDInflammatory Bowel Disease
CS-MaleInfMale Infertility
CS-WWSMuscular dystropy-dystroglycanopathy (Walker-Warburg)
CS-NephroticNephrotic Syndrome
CS-ObesityObesity
CS-PPK/CIPalmoplantar keratoderma / congenital ichthyosis
CS-PKDPolycystic Kidney Disease
CS-Primary ImmunodefPrimary Immunodeficiency
CS-RhabdoRhabdomyolysis
CS-SRTDShort-Rib Thoracic Dysplasia
CS-VACTERLVACTERL Association
CS-WSWaardenburg Syndrome

 
Nephrotic Syndrome

Select all: Gene symbolChrAvg % covered at 10xLocus TypeNoteOMIMPrevious symbol(s)Phenotype(s)Slice(s)
ACTN419q13.299.99%gene with protein product604638FSGS1Anemia; Autosomal dominant inheritance; Edema; Focal segmental glomerulosclerosis; Hyperlipidemia; Hypertension; Hypoalbuminemia; Incomplete penetrance; Proteinuria; Slow progression; Variable expressivityNephrotic Syndrome
ANLN7p14.299.94%gene with protein product616027Autosomal dominant inheritance; Focal segmental glomerulosclerosis; Nephrotic syndrome; Proteinuria; Stage 5 chronic kidney diseaseNephrotic Syndrome
APOL122q12.3100%gene with protein productCommon susceptibility alleles will not be reported.603743APOLNephrotic Syndrome
ARHGAP244q21.23-q21.100%gene with protein product610586Nephrotic Syndrome
ARHGDIA17q25.3100%gene with protein product601925GDIA1Autosomal recessive inheritance; Chronic kidney disease; Cortical visual impairment; Diffuse mesangial sclerosis; Edema; Hypoalbuminemia; Intellectual disability; Neonatal onset; Nephrotic syndrome; Proteinuria; Rapidly progressive; Sensorineural hearing impairment; Thin glomerular basement membraneNephrotic Syndrome
CD2AP6p12.399.67%gene with protein product604241Focal segmental glomerulosclerosis; Hematuria; Hypertension; Proteinuria; Renal insufficiencyNephrotic Syndrome
CFH1q31.399.83%gene with protein product134370HF, HF1, HF2Autosomal dominant inheritance; Autosomal recessive inheritance; Chronic kidney disease; Decreased serum complement factor H; Depletion of components of the alternative complement pathway; Glomerular subendothelial electron-dense deposits; Hematuria; Juvenile onset; Phenotypic variability; Progressive visual loss; Recurrent bacterial infections; Thickening of the glomerular basement membraneNephrotic Syndrome
COL4A32q36.3100%gene with protein product120070Anterior lenticonus; Anterior polar cataract; Autosomal dominant inheritance; Autosomal recessive inheritance; Azotemia; Cataract; Corneal erosion; Diffuse glomerular basement membrane lamellation; Glomerulonephritis; Hearing impairment; Hematuria; Heterogeneous; Hypertension; Hypophosphatemia; Lenticonus; Myopia; Nephritis; Nephrocalcinosis; Nephrotic syndrome; Nonprogressive; Progressive; Proteinuria; Sensorineural hearing impairment; Stage 5 chronic kidney disease; Thickening of the glomerular basement membrane; Thin glomerular basement membraneAlport Syndrome ; Nephrotic Syndrome
COL4A42q36.399.84%gene with protein product120131Anterior lenticonus; Autosomal recessive inheritance; Cataract; Corneal erosion; Diffuse glomerular basement membrane lamellation; Hearing impairment; Hematuria; Heterogeneous; Hypertension; Myopia; Nephritis; Nephrotic syndrome; Progressive; Proteinuria; Stage 5 chronic kidney disease; Thickening of the glomerular basement membraneAlport Syndrome ; Nephrotic Syndrome
COL4A5Xq22.399.93%gene with protein product303630ASLN, ATSAnterior lenticonus; Congenital cataract; Corneal erosion; Diffuse glomerular basement membrane lamellation; Diffuse leiomyomatosis; Heterogeneous; Hypertension; Hypoparathyroidism; Ichthyosis; Microscopic hematuria; Myopia; Nephritis; Nephrotic syndrome; Progressive; Proteinuria; Sensorineural hearing impairment; Stage 5 chronic kidney disease; Thickening of the glomerular basement membrane; Thrombocytopenia; X-linked dominant inheritanceAlport Syndrome ; Nephrotic Syndrome
COQ24q21.2399.98%gene with protein product609825Anemia; Ataxia; Autosomal recessive inheritance; Cerebellar atrophy; Dysarthria; Elevated serum creatine phosphokinase; Encephalopathy; Glomerulosclerosis; Hepatic failure; Hypergonadotropic hypogonadism; Hypertrophic cardiomyopathy; Intellectual disability; Lactic acidosis; Motor delay; Nephrotic syndrome; Nystagmus; Onset; Pancytopenia; Phenotypic variability; Postural instability; Progressive muscle weakness; Ragged-red muscle fibers; Recurrent myoglobinuria; Rod-cone dystrophy; Scanning speech; Seizures; Sensorineural hearing impairment; Specific learning disability; Visual lossNephrotic Syndrome
COQ614q24.3100%gene with protein product614647Autosomal recessive inheritance; Focal segmental glomerulosclerosis; Infantile onset; Nephrotic syndrome; Proteinuria; Rapidly progressive; Sensorineural hearing impairmentNephrotic Syndrome
COQ8B19q13.2100%gene with protein productFormer name = ADCK4615567ADCK4Autosomal recessive inheritance; Edema; Focal segmental glomerulosclerosis; Hypoalbuminemia; Nephrotic syndrome; Progressive; Proteinuria; Stage 5 chronic kidney diseaseNephrotic Syndrome
CRB29q33.3100%gene with protein product609720Autosomal recessive inheritance; Congenital onset; Focal segmental glomerulosclerosis; Hydrocephalus; Nephrotic syndrome; Polyhydramnios; Postaxial polydactyly; Renal corticomedullary cysts; Renal insufficiency; Seizures; VentriculomegalyNephrotic Syndrome
CUBN10p13100%gene with protein product602997MGA1Autosomal recessive inheritance; Childhood onset; Confusion; Dementia; Malabsorption of Vitamin B12; Megaloblastic anemia; Paresthesia; Proteinuria; Sensory impairmentNephrotic Syndrome
DGKE17q2299.99%gene with protein product601440Acute kidney injury; Autosomal recessive inheritance; Nephrotic syndrome; Progressive; Proteinuria; Thickening of the glomerular basement membraneNephrotic Syndrome
EMP216p13.13100%gene with protein product602334Autosomal recessive inheritance; Minimal change glomerulonephritis; Steroid-resistant nephrotic syndromeNephrotic Syndrome
FAT14q35.2100%gene with protein product600976FATNephrotic Syndrome
GSN9q33.299.99%gene with protein product137350Abnormality of abdomen morphology; Adult onset; Autosomal dominant inheritance; Bulbar palsy; Cardiac amyloidosis; Cardiomyopathy; Cutis laxa; Generalized amyloid deposition; Lattice corneal dystrophy; Nephrotic syndrome; Polyneuropathy; Renal insufficiencyNephrotic Syndrome
INF214q32.3393.62%gene with protein product610982C14orf151, C14orf173Areflexia; Autosomal dominant inheritance; Axonal loss; Distal lower limb amyotrophy; Distal muscle weakness; Distal sensory impairment; Distal upper limb amyotrophy; Focal segmental glomerulosclerosis; Foot dorsiflexor weakness; Hammertoe; Hyporeflexia; Nephrotic syndrome; Onion bulb formation; Pes cavus; Progressive; Proteinuria; Split hand; Steppage gaitAplastic Anemia ; Bone Marrow Failure Syndromes ; Nephrotic Syndrome
ITGA317q21.33100%gene with protein product605025MSK18Autosomal recessive inheritance; Decreased glomerular filtration rate; Fine hair; Fragile skin; Gynecomastia; Hypertelorism; Hypoalbuminemia; Macrotia; Microcephaly; Narrow chest; Narrow mouth; Neonatal respiratory distress; Phenotypic variability; Prominent forehead; Proteinuria; Renal insufficiency; Respiratory acidosis; Round face; Sparse and thin eyebrow; Sparse eyelashes; Sparse scalp hair; Tubular atrophyNephrotic Syndrome
ITGB417q25.1100%gene with protein product147557Abdominal distention; Abnormality of skin pigmentation; Abnormality of the genitourinary system; Abnormality of the stomach; Anemia; Anonychia; Aplasia cutis congenita; Aplasia of the bladder; Arthrogryposis multiplex congenita; Atrophic scars; Autosomal dominant inheritance; Autosomal recessive inheritance; Axillary pterygia; Camptodactyly of finger; Carious teeth; Congenital onset; Congenital pyloric atresia; Death in infancy; Dehydration; Dysphagia; Ectropion; Elevated maternal serum alpha-fetoprotein; Esophageal atresia; Failure to thrive; Fragile nails; Fragile skin; Glomerulosclerosis; Hematuria; Heterogeneous; Hydronephrosis; Hypodontia; Hypoplasia of dental enamel; Intestinal atresia; Intractable diarrhea; Junctional split; Limitation of joint mobility; Milia; Nail dysplasia; Nail dystrophy; Nausea and vomiting; Oral mucosal blisters; Palmar hyperhidrosis; Palmoplantar blistering; Plantar hyperkeratosis; Polyhydramnios; Premature birth; Recurrent skin infections; Renal duplication; Renal dysplasia; Scarring alopecia of scalp; Sepsis; Skin erosion; Sparse body hair; Ureterocele; Urethral stricture; Urinary bladder inflammationNephrotic Syndrome ; Palmoplantar keratoderma / congenital ichthyosis
KANK19p24.3100%gene with protein product607704ANKRD15Autosomal dominant inheritance with maternal imprinting; Cerebral atrophy; Cerebral palsy; Intellectual disability; Muscular hypotonia; Spastic tetraplegia; VentriculomegalyNephrotic Syndrome
KANK219p13.2100%gene with protein product614610MXRA3, ANKRD25Autosomal recessive inheritance; Palmoplantar keratoderma; Sparse and thin eyebrow; Sparse body hair; Sparse eyelashes; Sparse scalp hair; Woolly hair; Woolly scalp hairNephrotic Syndrome ; Palmoplantar keratoderma / congenital ichthyosis
KANK41p31.399.99%gene with protein product614612ANKRD38Nephrotic Syndrome
LAMB23p21.31100%gene with protein product150325LAMSAreflexia; Autosomal recessive inheritance; Blindness; Diffuse mesangial sclerosis; Edema; Generalized hypotonia; Hypoplasia of the ciliary body; Hypoplasia of the iris; Hypoproteinemia; Myopia; Neonatal onset; Nephrotic syndrome; Nystagmus; Posterior lenticonus; Proteinuria; Stage 5 chronic kidney disease; StrabismusNephrotic Syndrome
LMX1B9q33.399.76%gene with protein product602575NPS1Abnormality of the fingernails; Absence of pectoralis minor muscle; Absent distal interphalangeal creases; Anonychia; Antecubital pterygium; Aplasia/Hypoplasia of the patella; Autosomal dominant inheritance; Biceps aplasia; Cataract; Cleft palate; Cleft upper lip; Clinodactyly of the 5th finger; Concave nail; Cubitus valgus; Disproportionate prominence of the femoral medial condyle; Elongated radius; Exostoses; Glaucoma; Glenoid fossa hypoplasia; Glomerulonephritis; Hematuria; Hypoplasia of first ribs; Hypoplastic radial head; Hypoplastic toenails; Iliac horns; Joint hyperflexibility; Joint stiffness; Joint swelling; Keratoconus; Limited elbow extension; Lumbar hyperlordosis; Microcornea; Microphakia; Nephrotic syndrome; Osteoarthritis; Patellar aplasia; Patellar dislocation; Pectus excavatum; Pes planus; Proteinuria; Ptosis; Quadriceps aplasia; Renal insufficiency; Ridged nail; Scoliosis; Sensorineural hearing impairment; Short stature; Skeletal dysplasia; Spina bifida; Talipes equinovarus; Thickening of the lateral border of the scapula; Triceps aplasiaNephrotic Syndrome
MAGI27q21.1199.4%gene with protein product606382Nephrotic Syndrome
MYO1E15q22.299.95%gene with protein product601479Autosomal recessive inheritance; Chronic kidney disease; Edema; Focal segmental glomerulosclerosis; Hematuria; Hypoalbuminemia; Nephrotic syndrome; Progressive; Proteinuria; Tubular atrophyNephrotic Syndrome
NPHP12q1398.95%gene with protein product607100NPH1Abnormal electroretinogram; Abnormality of retinal pigmentation; Anemia; Apnea; Ataxia; Autosomal recessive inheritance; Biparietal narrowing; Cerebellar vermis hypoplasia; Cognitive impairment; Delayed gross motor development; Elongated superior cerebellar peduncle; Feeding difficulties; Gait disturbance; Generalized hypotonia; Global developmental delay; Growth delay; Heterogeneous; Hypertension; Hypogonadism; Hypometric saccades; Hypoplasia of penis; Hypoplasia of the ovary; Hyposthenuria; Intellectual disability; Long face; Low-set, posteriorly rotated ears; Molar tooth sign on MRI; Multicystic kidney dysplasia; Muscular hypotonia; Nephronophthisis; Nephropathy; Nystagmus; Obesity; Oculomotor apraxia; Pigmentary retinopathy; Polydipsia; Polyuria; Postaxial hand polydactyly; Premature ovarian insufficiency; Progressive visual loss; Renal corticomedullary cysts; Renal insufficiency; Retinal dystrophy; Short stature; Stage 5 chronic kidney disease; Tapetoretinal degeneration; Thickened superior cerebellar peduncle; Tubular atrophy; Tubular basement membrane disintegration; Tubulointerstitial fibrosis; Visual impairmentHeterotaxy ; Nephrotic Syndrome
NPHS119q13.12100%gene with protein product602716Abdominal distention; Abnormality of the renal tubule; Autosomal recessive inheritance; Congenital nephrotic syndrome; Congenital onset; Delayed eruption of permanent teeth; Diffuse mesangial sclerosis; Edema; Elevated amniotic fluid alpha-fetoprotein; Gastroesophageal reflux; Growth delay; Hyperlipidemia; Hypoalbuminemia; Hypoproteinemia; Hypothyroidism; Neonatal respiratory distress; Nephrotic syndrome; Proteinuria; Pyloric stenosis; Rapidly progressive; Recurrent infections; Renal insufficiency; Small for gestational age; Tubular atrophyNephrotic Syndrome
NPHS21q25.2100%gene with protein product604766Autosomal recessive inheritance; Edema; Focal segmental glomerulosclerosis; Hyperlipidemia; Hypoalbuminemia; Juvenile onset; Nephrotic syndrome; Proteinuria; Rapidly progressive; Stage 5 chronic kidney disease; Variable expressivityNephrotic Syndrome
NUP10712q1599.88%gene with protein product607617Aplasia/Hypoplasia of the breasts; Aplasia/hypoplasia of the uterus; Autosomal recessive inheritance; Cognitive impairment; Decreased fertility; Decreased serum estradiol; Delayed puberty; Delayed skeletal maturation; EEG abnormality; Global developmental delay; Gonadal dysgenesis; Hiatus hernia; Hypoalbuminemia; Hypoplasia of the ear cartilage; Increased circulating gonadotropin level; Intrauterine growth retardation; Macrotia; Microcephaly; Minimal change glomerulonephritis; Nephropathy; Nephrotic syndrome; Osteopenia; Osteoporosis of vertebrae; Pachygyria; Premature birth; Premature ovarian insufficiency; Primary amenorrhea; Progressive; Proteinuria; Seizures; Short stature; Sparse pubic hair; Stage 5 chronic kidney disease; Streak ovary; Variable expressivityNephrotic Syndrome
NUP2057q33100%gene with protein product614352C7orf14Autosomal recessive inheritance; Focal segmental glomerulosclerosis; Stage 5 chronic kidney disease; Steroid-resistant nephrotic syndromeNephrotic Syndrome
NUP9316q13100%gene with protein product614351Autosomal recessive inheritance; Diffuse mesangial sclerosis; Hematuria; Progressive; Stage 5 chronic kidney diseaseNephrotic Syndrome
PAX210q24.31100%gene with protein product167409Abnormality of the foot; Arnold-Chiari type I malformation; Autosomal dominant inheritance; Autosomal recessive inheritance; Bicornuate uterus; Chorioretinal atrophy; Congenital onset; Focal segmental glomerulosclerosis; Gliosis; Hyperextensible skin; Hypertelorism; Hypertension; Incomplete penetrance; Infantile onset; Intellectual disability; Joint laxity; Low-set ears; Microphthalmia; Morning glory anomaly; Multicystic kidney dysplasia; Myopia; Nephrotic syndrome; Oligohydramnios; Optic nerve coloboma; Optic nerve dysplasia; Orbital cyst; Phenotypic variability; Potter facies; Primary amenorrhea; Proteinuria; Pulmonary hypoplasia; Renal agenesis; Renal dysplasia; Renal hypoplasia; Renal insufficiency; Retinal coloboma; Retrognathia; Seizures; Sensorineural hearing impairment; Soft skin; Stage 5 chronic kidney disease; Talipes equinovarus; Vaginal atresia; Variable expressivity; Vesicoureteral reflux; Visual impairmentCongenital Kidney and Urinary Tract (CKUT) Anomalies; Nephrotic Syndrome
PDSS26q2199.94%gene with protein product610564C6orf210Autosomal recessive inheritance; Cortical visual impairment; Edema; Feeding difficulties; Increased serum lactate; Neonatal hypotonia; Nephrotic syndrome; Proteinuria; Status epilepticusNephrotic Syndrome
PLCE110q23.3399.98%gene with protein product608414Autosomal recessive inheritance; Childhood onset; Diffuse mesangial sclerosis; Edema; Focal segmental glomerulosclerosis; Hypoalbuminemia; Nephrotic syndrome; Progressive; Proteinuria; Stage 5 chronic kidney diseaseNephrotic Syndrome
PTPRO12p12.399.48%gene with protein product600579Autosomal recessive inheritance; Edema; Focal segmental glomerulosclerosis; Hypoalbuminemia; Nephrotic syndrome; Proteinuria; Tubulointerstitial fibrosis; Variable expressivityNephrotic Syndrome
SGPL110q22.1100%gene with protein product603729Nephrotic Syndrome
SMARCAL12q35100%gene with protein product606622Abnormal immunoglobulin level; Abnormal T cell morphology; Abnormality of epiphysis morphology; Anemia; Arteriosclerosis; Astigmatism; Autosomal recessive inheritance; Bulbous nose; Cellular immunodeficiency; Coarse hair; Depressed nasal bridge; Disproportionate short-trunk short stature; Fine hair; Focal segmental glomerulosclerosis; Glomerulopathy; High pitched voice; Hip dislocation; Hyperlordosis; Hypermelanotic macule; Hypertension; Hypoplasia of the capital femoral epiphysis; Increased thyroid-stimulating hormone level; Intrauterine growth retardation; Lateral displacement of the femoral head; Lumbar hyperlordosis; Lymphopenia; Melanocytic nevus; Microdontia; Motor delay; Multiple cafe-au-lait spots; Myopia; Nephrotic syndrome; Neutropenia; Opacification of the corneal stroma; Osteopenia; Ovoid vertebral bodies; Platyspondyly; Proteinuria; Protuberant abdomen; Recurrent infections; Renal insufficiency; Shallow acetabular fossae; Short neck; Spondyloepiphyseal dysplasia; Thoracic kyphosis; Thrombocytopenia; Transient ischemic attack; Waddling gaitNephrotic Syndrome
TRPC611q22.197.29%gene with protein product603652FSGS2Chronic kidney disease; Focal segmental glomerulosclerosis; Nephrotic syndrome; ProteinuriaNephrotic Syndrome
TTC21B2q24.399.99%gene with protein product612014Abnormality of pelvic girdle bone morphology; Abnormality of the clavicle; Abnormality of the metaphysis; Abnormality of the ribs; Abnormality of the sternum; Autosomal dominant inheritance; Autosomal recessive inheritance; Brachydactyly; Cone-shaped epiphysis; Micromelia; Narrow chest; Nephronophthisis; Respiratory insufficiency; Retinal degeneration; Short foot; Short long bone; Short ribs; Short stature; Short thorax; Skeletal dysplasia; Stage 5 chronic kidney diseaseHeterotaxy ; Nephrotic Syndrome ; Short-Rib Thoracic Dysplasia
WT111p13100%gene with protein product607102GUDAbdominal distention; Abdominal pain; Abnormal sex determination; Abnormality of the fallopian tube; Abnormality of the labia; Abnormality of the peritoneum; Abnormality of the scrotum; Abnormality of the vagina; Ambiguous genitalia; Ambiguous genitalia, female; Ambiguous genitalia, male; Aniridia; Aplasia/Hypoplasia of the iris; Aplasia/Hypoplasia of the lungs; Autosomal dominant inheritance; Autosomal recessive inheritance; Azoospermia; Cataract; Childhood onset; Clitoral hypertrophy; Congenital diaphragmatic hernia; Contiguous gene syndrome; Cryptorchidism; Decreased fertility in females; Decreased serum estradiol; Decreased testicular size; Decreased testosterone in males; Delayed puberty; Diffuse mesangial sclerosis; Displacement of the external urethral meatus; Elevated circulating follicle stimulating hormone level; Elevated circulating luteinizing hormone level; Everted lower lip vermilion; Female external genitalia in individual with 46,XY karyotype; Focal segmental glomerulosclerosis; Glaucoma; Glomerulopathy; Gonadal dysgenesis; Gonadal dysgenesis with female appearance, male; Gonadal tissue inappropriate for external genitalia or chromosomal sex; Gonadoblastoma; Gynecomastia; Hearing abnormality; Hepatomegaly; Heterogeneous; Hydrometrocolpos; Hypergonadotropic hypogonadism; Hypertension; Hypogonadotrophic hypogonadism; Hypoplasia of penis; Hypoplasia of the corpus callosum; Hypoplasia of the fovea; Hypoplasia of the vagina; Hypoplastic left heart; Hypospadias; Ileus; Increased circulating gonadotropin level; Intellectual disability; Male infertility; Male pseudohermaphroditism; Malignant mesothelioma; Mediastinal lymphadenopathy; Microcephaly; Micrognathia; Micropenis; Nausea and vomiting; Nephroblastoma; Nephropathy; Nephrotic syndrome; Nystagmus; Opacification of the corneal stroma; Optic nerve hypoplasia; Osteoporosis; Ovarian gonadoblastoma; Polycystic ovaries; Primary amenorrhea; Progressive; Proteinuria; Ptosis; Pulmonary sequestration; Renal insufficiency; Sarcoma; Short stature; Somatic mutation; Sparse axillary hair; Sparse pubic hair; Stage 5 chronic kidney disease; Streak ovary; Testicular dysgenesis; True hermaphroditism; Urogenital sinus anomaly; Vaginal atresia; Vanishing testis; Visual impairmentCongenital Kidney and Urinary Tract (CKUT) Anomalies; Disorders of Sex Development; Nephrotic Syndrome
XPO56p21.1100%gene with protein product607845Nephrotic Syndrome

The gene coverage data provided by GeneDx represent an estimate based on previous results, but the specific sequencing coverage data for the genes selected may vary from individual to individual, and cannot be predicted exactly. Changes to an approved gene list can only be made by contacting GeneDx directly at 888-729-1206 and asking to speak with a member of our Whole Exome Sequencing Laboratory.