RS3914132 Unknown gene
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What This Variant Does
"Each C allele at rs3914132 decreases the likelihood of developing otosclerosis, which can cause hear..."
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Otosclerosis | — | OR: 1.54 | 2E-8 | PubMed |