RS56211063 Unknown gene

Other Chr 9:114823617
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What This Variant Does
"Human primary biliary cirrhosis-susceptible allele of rs4979462 enhances TNFSF15 expression by binding NF-1"
GWAS Studies (5)
Trait Risk Allele OR / Beta P-value Study
Crohn's disease — OR: 0.55 4E-142 PubMed
Crohn's disease C OR: 2.09 4E-95 PubMed
Inflammatory bowel disease — OR: 0.33 3E-89 PubMed
Primary biliary cholangitis C OR: 0.44 9E-26 PubMed
Ulcerative colitis — OR: 0.14 5E-12 PubMed
Ask Dr. Hemsworth about this variant