RS7865618 Unknown gene

Other Chr 9:22031006
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs7865618 increases susceptibility to Coronary artery disease 1.23 times for heterozygotes (AG) and ..."
GWAS Studies (4)
Trait Risk Allele OR / Beta P-value Study
Coronary heart disease A OR: 1.18 2E-27 PubMed
Vertical cup-disc ratio G β: 0.013 5E-24 PubMed
Optic cup area G β: 0.024 9E-20 PubMed
Glaucoma (primary open-angle) A OR: 1.78 9E-11 PubMed
Ask Dr. Hemsworth about this variant