RS756484720 GJB2

Health Risk Chr 13:20189247
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Hearing loss
Rare genetic deafness
Nonsyndromic genetic hearing loss
8 conditions
Monogenic hearing loss
Autosomal recessive nonsyndromic hearing loss 1A
Hearing loss
Rare genetic deafness
Nonsyndromic genetic hearing loss
8 conditions
Monogenic hearing loss
Other Variants in GJB2
rs35887622 rs80338944 rs104894396 rs104894397 rs80338939 rs104894398 rs80338947 rs80338950 rs80338948 rs80338942
Ask Dr. Hemsworth about this variant