RS727503493 TMPRSS3
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 8
Inborn genetic diseases
Hearing impairment
TMPRSS3-related disorder
Nonsyndromic genetic hearing loss
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 8
Inborn genetic diseases
Hearing impairment
TMPRSS3-related disorder
Nonsyndromic genetic hearing loss
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Age-related hearing impairment | T | OR: 1.49 | 8E-8 | PubMed |
Other Variants in TMPRSS3