RS111033204 GJB2
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What This Variant Does
"Prevalent connexin 26 gene (GJB2) mutations in Japanese. Connexin26 mutations associated with nonsyn...
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 1B
8 conditions
Autism spectrum disorder
CREBBP-related disorder
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 1B
8 conditions
Autism spectrum disorder
CREBBP-related disorder
Other Variants in GJB2