RS111033297 GJB2

Health Risk Chr 13:20189412 snv stop gained
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 1A
Hearing loss
GJB2-related disorder
7 conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 1A
Hearing loss
GJB2-related disorder
7 conditions
Population Frequencies
gnomAD ALL
100%
Other Variants in GJB2
rs35887622 rs80338944 rs104894396 rs104894397 rs80338939 rs104894398 rs80338947 rs80338950 rs80338948 rs80338942
Ask Dr. Hemsworth about this variant