rs10167219
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10167219(C;C) |
| Make rs10167219(C;T) |
| Make rs10167219(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 226275057 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10167219 |
| dbSNP (classic) | rs10167219 |
| ClinGen | rs10167219 |
| ebi | rs10167219 |
| HLI | rs10167219 |
| Exac | rs10167219 |
| Gnomad | rs10167219 |
| Varsome | rs10167219 |
| LitVar | rs10167219 |
| Map | rs10167219 |
| PheGenI | rs10167219 |
| Biobank | rs10167219 |
| 1000 genomes | rs10167219 |
| hgdp | rs10167219 |
| ensembl | rs10167219 |
| geneview | rs10167219 |
| scholar | rs10167219 |
| rs10167219 | |
| pharmgkb | rs10167219 |
| gwascentral | rs10167219 |
| openSNP | rs10167219 |
| 23andMe | rs10167219 |
| SNPshot | rs10167219 |
| SNPdbe | rs10167219 |
| MSV3d | rs10167219 |
| GWAS Ctlg | rs10167219 |
| GMAF | 0.2704 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 23659870
] Common variants in and near IRS1 and subclinical cardiovascular disease in the Framingham Heart Study
