RS7848647 Unknown gene

Other Chr 9:114806766
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What This Variant Does
"Associated with increased risk for Crohn's disease in a study of 380 Korean patients. [OMIM:INFLAMM..."
GWAS Studies (3)
Trait Risk Allele OR / Beta P-value Study
Inflammatory bowel disease 3E-35 PubMed
Chronic inflammatory diseases (ankylosing spondylitis, Crohn's disease, psoriasis, primary sclerosing cholangitis, ulcerative colitis) (pleiotropy) 1E-25 PubMed
Pediatric steroid sensitive nephrotic syndrome T OR: 0.7 1E-12 PubMed
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