rs11190164
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common/normal |
| Make rs11190164(A;G) |
| Make rs11190164(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 10 |
| Position | 99591947 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11190164 |
| dbSNP (classic) | rs11190164 |
| ClinGen | rs11190164 |
| ebi | rs11190164 |
| HLI | rs11190164 |
| Exac | rs11190164 |
| Gnomad | rs11190164 |
| Varsome | rs11190164 |
| LitVar | rs11190164 |
| Map | rs11190164 |
| PheGenI | rs11190164 |
| Biobank | rs11190164 |
| 1000 genomes | rs11190164 |
| hgdp | rs11190164 |
| ensembl | rs11190164 |
| geneview | rs11190164 |
| scholar | rs11190164 |
| rs11190164 | |
| pharmgkb | rs11190164 |
| gwascentral | rs11190164 |
| openSNP | rs11190164 |
| 23andMe | rs11190164 |
| SNPshot | rs11190164 |
| SNPdbe | rs11190164 |
| MSV3d | rs11190164 |
| GWAS Ctlg | rs11190164 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 29403313
] Strongly enhanced colorectal cancer risk stratification by combining family history and genetic risk score
