RS397516874 GJB2

Health Risk Chr 13:20189212
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Hearing loss
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Hearing loss
Other Variants in GJB2
rs35887622 rs80338944 rs104894396 rs104894397 rs80338939 rs104894398 rs80338947 rs80338950 rs80338948 rs80338942
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