RS121908932 COCH
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 9
Rare genetic deafness
Hereditary hearing loss and deafness
Autosomal dominant nonsyndromic hearing loss 9
Autosomal dominant nonsyndromic hearing loss 9
Rare genetic deafness
Hereditary hearing loss and deafness
Autosomal dominant nonsyndromic hearing loss 9
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Hearing loss | — | OR: 81.39 | 2E-12 | PubMed |
Other Variants in COCH