RS2066845 NOD2

Health Risk Chr 16:50722629
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What This Variant Does
"rs2066845 is a SNP in the NOD2 gene
Associated Conditions
Blau syndrome
Yao syndrome
Inflammatory bowel disease 1
Psoriatic arthritis
susceptibility to
Regional enteritis
Autoinflammatory syndrome
Blau syndrome
Inflammatory bowel disease 1
Regional enteritis
Blau syndrome
Yao syndrome
Inflammatory bowel disease 1
Psoriatic arthritis
susceptibility to
GWAS Studies (2)
Trait Risk Allele OR / Beta P-value Study
Chronic inflammatory diseases (ankylosing spondylitis, Crohn's disease, psoriasis, primary sclerosing cholangitis, ulcerative colitis) (pleiotropy) — — 6E-94 PubMed
Crohns disease C OR: 0.91 1E-11 PubMed
Other Variants in NOD2
rs2066847 rs2066844 rs104895461 rs104895460 rs104895462 rs5743289 rs104895472 rs104895476 rs104895438 rs104895477
Ask Dr. Hemsworth about this variant