RS80338940 GJB2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Hearing impairment
Rare genetic deafness
Hearing loss
Autosomal recessive nonsyndromic hearing loss 1B
Nonsyndromic genetic hearing loss
autosomal recessive
Ear malformation
Autosomal dominant nonsyndromic hearing loss 3A
Autosomal recessive nonsyndromic hearing loss 104
GJB2-related disorder
Mutilating keratoderma
Palmoplantar keratoderma-deafness syndrome
Knuckle pads
deafness AND leukonychia syndrome
Other Variants in GJB2