rs2217332
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2217332(C;C) |
| Make rs2217332(C;T) |
| Make rs2217332(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 56935236 |
| Gene | HERPUD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2217332 |
| dbSNP (classic) | rs2217332 |
| ClinGen | rs2217332 |
| ebi | rs2217332 |
| HLI | rs2217332 |
| Exac | rs2217332 |
| Gnomad | rs2217332 |
| Varsome | rs2217332 |
| LitVar | rs2217332 |
| Map | rs2217332 |
| PheGenI | rs2217332 |
| Biobank | rs2217332 |
| 1000 genomes | rs2217332 |
| hgdp | rs2217332 |
| ensembl | rs2217332 |
| geneview | rs2217332 |
| scholar | rs2217332 |
| rs2217332 | |
| pharmgkb | rs2217332 |
| gwascentral | rs2217332 |
| openSNP | rs2217332 |
| 23andMe | rs2217332 |
| SNPshot | rs2217332 |
| SNPdbe | rs2217332 |
| MSV3d | rs2217332 |
| GWAS Ctlg | rs2217332 |
| GMAF | 0.1166 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20694148 ]
|
| Trait | |
| Title | A genome-wide association study of the metabolic syndrome in Indian Asian men |
| Risk Allele | |
| P-val | 0.000003 |
| Odds Ratio | None None |
[PMID 20031564] Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study.
[PMID 26823705] Evidence of a novel gene HERPUD1 in polypoidal choroidal vasculopathy.
