rs4971092
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4971092(C;C) |
| Make rs4971092(C;T) |
| Make rs4971092(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 155171470 |
| Gene | KRTCAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4971092 |
| dbSNP (classic) | rs4971092 |
| ClinGen | rs4971092 |
| ebi | rs4971092 |
| HLI | rs4971092 |
| Exac | rs4971092 |
| Gnomad | rs4971092 |
| Varsome | rs4971092 |
| LitVar | rs4971092 |
| Map | rs4971092 |
| PheGenI | rs4971092 |
| Biobank | rs4971092 |
| 1000 genomes | rs4971092 |
| hgdp | rs4971092 |
| ensembl | rs4971092 |
| geneview | rs4971092 |
| scholar | rs4971092 |
| rs4971092 | |
| pharmgkb | rs4971092 |
| gwascentral | rs4971092 |
| openSNP | rs4971092 |
| 23andMe | rs4971092 |
| SNPshot | rs4971092 |
| SNPdbe | rs4971092 |
| MSV3d | rs4971092 |
| GWAS Ctlg | rs4971092 |
| GMAF | 0.06244 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19924550
] A comprehensive analysis of common genetic variation in MUC1, MUC5AC, MUC6 genes and risk of stomach cancer
