RS111033451 GJB2

Health Risk Chr 13:20189563
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Inborn genetic diseases
7 conditions
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Inborn genetic diseases
7 conditions
Other Variants in GJB2
rs35887622 rs80338944 rs104894396 rs104894397 rs80338939 rs104894398 rs80338947 rs80338950 rs80338948 rs80338942
Ask Dr. Hemsworth about this variant