RS1064797088 GJB2

Health Risk Chr 13:20189446
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 3A
Autosomal dominant nonsyndromic hearing loss 3A
Other Variants in GJB2
rs35887622 rs80338944 rs104894396 rs104894397 rs80338939 rs104894398 rs80338947 rs80338950 rs80338948 rs80338942
Ask Dr. Hemsworth about this variant