rs1799762
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 0 |
| Make rs1799762(-;G) |
| Make rs1799762(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 101126426 |
| Gene | SERPINE1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1799762 |
| dbSNP (classic) | rs1799762 |
| ClinGen | rs1799762 |
| ebi | rs1799762 |
| HLI | rs1799762 |
| Exac | rs1799762 |
| Gnomad | rs1799762 |
| Varsome | rs1799762 |
| LitVar | rs1799762 |
| Map | rs1799762 |
| PheGenI | rs1799762 |
| Biobank | rs1799762 |
| 1000 genomes | rs1799762 |
| hgdp | rs1799762 |
| ensembl | rs1799762 |
| geneview | rs1799762 |
| scholar | rs1799762 |
| rs1799762 | |
| pharmgkb | rs1799762 |
| gwascentral | rs1799762 |
| openSNP | rs1799762 |
| 23andMe | rs1799762 |
| SNPshot | rs1799762 |
| SNPdbe | rs1799762 |
| MSV3d | rs1799762 |
| GWAS Ctlg | rs1799762 |
| Merged from | Rs34857375, Rs72578597 |
| GMAF | 0.4683 |
| Max Magnitude | 0 |
This SNP is equivalent to, and therefore please go to, rs1799889 for related information.
[PMID 18603647
] Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response.
[PMID 18805939] Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.
[PMID 18936436] Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994.
[PMID 23274712] Genetic polymorphisms and the risk of myocardial infarction in patients under 45 years of age.
[PMID 30515004] Association Between - 675 ID, 4G/5G PAI-1 Gene Polymorphism and Pregnancy Loss: A Systematic Review.
