RS587783647 GJB2
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What This Variant Does
"CLNSIG=255
Associated Conditions
Hearing impairment
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 3A
Inborn genetic diseases
GJB2-related disorder
7 conditions
Hearing impairment
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 3A
Inborn genetic diseases
GJB2-related disorder
7 conditions
Other Variants in GJB2