RS35887622 GJB2
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What This Variant Does
"rs35887622 represents a relatively frequent variant that was originally reported to be associated wi...
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Nonsyndromic genetic hearing loss
Autosomal dominant nonsyndromic hearing loss 3A
Hearing loss
Autosomal recessive nonsyndromic hearing loss 1B
Rare genetic deafness
Nonsyndromic Deafness
7 conditions
Inborn genetic diseases
Hearing impairment
See cases
Autosomal dominant keratitis-ichthyosis-hearing loss syndrome
GJB2-related disorder
Monogenic hearing loss
Rare genetic deafness
GWAS Studies (2)
Other Variants in GJB2