Rs2327832
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs2327832 |
| hapmap | rs2327832 |
| hgdp | rs2327832 |
| ensembl | rs2327832 |
| gopubmed | rs2327832 |
| scholar | rs2327832 |
| rs2327832 | |
| pharmgkb | rs2327832 |
| hgvbaseg2p | rs2327832 |
| medrefsnp | rs2327832 |
| 23andMe | rs2327832 |
| SNP Nexus |
| Chromosome | 6 |
| Orientation | plus |
| Position | 137973068 |
| Reference | GRCh37 37.1/131 |
| Genotype | Effect |
|---|---|
| rs2327832(A;A)* | ? |
| rs2327832(A;G)* | ? |
| rs2327832(G;G)* | ? |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19240061] Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling
| GWAS snp | |
|---|---|
| PMID | [PMID 20190752] |
| Trait | Celiac disease |
| Title | Multiple common variants for celiac disease influencing immune gene expression |
| Risk Allele | G |
| P-val | 4E-19 |
| Odds Ratio | 1.23 [1.17-1.28] |
