RS6730839 Unknown gene

Other Chr ?:?
Upload your DNA to see your genotype for this variant.
GWAS Studies (2)
Trait Risk Allele OR / Beta P-value Study
Inguinal hernia G OR: 1.18 5E-28 PubMed
Disorders of optic nerve and visual pathways (PheCode 377) G OR: 0.11 2E-13 PubMed
Ask Dr. Hemsworth about this variant