rs11988997
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) |
| Make rs11988997(C;C) |
| Make rs11988997(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 118753955 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11988997 |
| dbSNP (classic) | rs11988997 |
| ClinGen | rs11988997 |
| ebi | rs11988997 |
| HLI | rs11988997 |
| Exac | rs11988997 |
| Gnomad | rs11988997 |
| Varsome | rs11988997 |
| LitVar | rs11988997 |
| Map | rs11988997 |
| PheGenI | rs11988997 |
| Biobank | rs11988997 |
| 1000 genomes | rs11988997 |
| hgdp | rs11988997 |
| ensembl | rs11988997 |
| geneview | rs11988997 |
| scholar | rs11988997 |
| rs11988997 | |
| pharmgkb | rs11988997 |
| gwascentral | rs11988997 |
| openSNP | rs11988997 |
| 23andMe | rs11988997 |
| SNPshot | rs11988997 |
| SNPdbe | rs11988997 |
| MSV3d | rs11988997 |
| GWAS Ctlg | rs11988997 |
| GMAF | 0.06933 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23143602 ]
|
| Trait | Pancreatitis |
| Title | Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. |
| Risk Allele | T |
| P-val | 6E-6 |
| Odds Ratio | 1.36 [1.21-1.50] |
