Genetic Testing Company | The DNA Diagnostic Experts | GeneDx

In observance of the holiday, GeneDx will be closed for business on Thursday, November 27, 2014, and will be unable to receive and process specimens. FedEx and UPS will also not operate. We will accept specimens on Friday, November 28, and  will resume our normal work schedule on Saturday, November 29, 2014.  If you have any questions or inquiries, please call us at 301-519-2100 or email us at zebras@genedx.com.

SAG Remaining Exon Sequencing

FORMS AND DOCUMENTS

TEST DETAILS

Genes:
SAG
Disorders:
Clinical Utility:
  • Confirmation of a clinical diagnosis.
  • Development of an appropriate management plan.
  • Prenatal diagnosis in families with a defined mutation
Lab Method:
Capillary Sequencing

ORDERING

Test Code:
518
Turnaround Time:
6-7 weeks
Preferred Specimen:
2-5 mL Blood - Lavender Top Tube

BILLING

CPT Codes:
81479x1
New York Approved:
No
ABN Required:
Yes
Billing Information:
View Billing Policy
ICD Codes:
  • 368.61: Congenital night blindness, Hereditary night blindness, Oguchi's disease
  • 368.63: Abnormal dark adaptation curve, Abnormal threshold of cones or rods, Delayed adaptation of cones or rods
* For price inquiries please email zebras@genedx.com

REFERENCES

  1. al-Jandal et al., (1999) Human Mutation 13:75-81
  2. Dryja et al., (1993) Nat Genet 4:280-283
  3. Yamamoto H et al., (1999) Nat Genet 22:188-91
  4. Nakamura et al. (2003) Doc Ophthalmol 107(1):3-11
  5. Nakamura et al., (2000) Invest Ophthalmol Vis Sci 41(12):3925-32
  6. Yamamoto et al., (1997) Nat Genet 15(2):175-178
  7. Nakamura et al., (2004) American Academy of Ophthalmology 111(7):1410-1414
  8. Nakazawa et al., (1998) Arch Ophthalmol 116:498-501
  9. Fuchs et al., (1995) Nat Genet 10:360-362
  10. Li et al., (2009) Am J Hum Genet 85:711-719
  11. Audo et al., (2009) Am J Hum Genet 85: 720- 729
  12. Bech-Hansen et al., (2000) Nat Genet 26: 319-323
  13. Pusch et al., (2000) Nat Genet 26:324-327
  14. Xiao et al., (2006) J Hum Genet 51:634-640
  15. van Genderen et al., (2009) Am J Hum Genet 85: 730-736

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