RS1057517521 GJB2
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 3A
Autosomal recessive nonsyndromic hearing loss 1A
GJB2-related disorder
Monogenic hearing loss
Autosomal dominant nonsyndromic hearing loss 3A
Autosomal recessive nonsyndromic hearing loss 1A
GJB2-related disorder
Monogenic hearing loss
Other Variants in GJB2