RS2066847 NOD2
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What This Variant Does
"rs2066847 is one of several SNPs referring to a one base insertion into a run of C's within exon 11 ...
Associated Conditions
Yao syndrome
Blau syndrome
Inflammatory bowel disease 1
Crohn’s Disease
Autoinflammatory syndrome
Regional enteritis
Crohn disease
Yao syndrome
Blau syndrome
Inflammatory bowel disease 1
Crohn’s Disease
Autoinflammatory syndrome
Regional enteritis
Crohn disease
GWAS Studies (7)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Crohn's disease | T | OR: 3.1 | 6E-209 | PubMed |
| Crohns disease | GC | OR: 1.08 | 2E-24 | PubMed |
| Crohn's disease | C | OR: 3.99 | 3E-24 | PubMed |
| Crohn's disease | — | OR: 1.62 | 2E-15 | PubMed |
| Age of onset of childhood onset asthma | — | OR: 0.24 | 1E-9 | PubMed |
| Inflammatory bowel disease | G | OR: 0.71 | 2E-9 | PubMed |
| ICD10 K50, K51: inflammatory bowel disease | — | OR: 1.46 | 2E-9 | PubMed |
Other Variants in NOD2