RS9938149 Unknown gene

Other Chr 16:88298034
Upload your DNA to see your genotype for this variant.
What This Variant Does
"Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease..."
GWAS Studies (3)
Trait Risk Allele OR / Beta P-value Study
Corneal structure A OR: 0.17 2E-49 PubMed
Intraocular pressure C OR: 0.14 4E-24 PubMed
Central corneal thickness A OR: 0.16 1E-12 PubMed
Ask Dr. Hemsworth about this variant