RS111033217 GJB2

Health Risk Chr 13:20189537 snv missense variant
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
7 conditions
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
7 conditions
Population Frequencies
gnomAD ALL
100%
Other Variants in GJB2
rs35887622 rs80338944 rs104894396 rs104894397 rs80338939 rs104894398 rs80338947 rs80338950 rs80338948 rs80338942
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