RS80338939 GJB2
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What This Variant Does
"rs80338939, also known as 35delG or in some cases 30delG, is a SNP in the GJB2 gene. This variant is...
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Deafness
digenic
GJB2/GJB6
Hearing impairment
Nonsyndromic genetic hearing loss
Bilateral conductive hearing impairment
7 conditions
Autosomal dominant nonsyndromic hearing loss 3A
Bilateral sensorineural hearing impairment
Severe sensorineural hearing impairment
Inborn genetic diseases
Hearing loss
Autosomal recessive nonsyndromic hearing loss 1B
Rare genetic deafness
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Hearing loss | — | OR: 1.21 | 4E-11 | PubMed |
Other Variants in GJB2