rs3819102
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs3819102(C;C) |
| Make rs3819102(C;T) |
| Reference | GRCh37 37.1/131 |
| Chromosome | 18 |
| Position | 675307 |
| Gene | ENOSF1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3819102 |
| dbSNP (classic) | rs3819102 |
| ClinGen | rs3819102 |
| ebi | rs3819102 |
| HLI | rs3819102 |
| Exac | rs3819102 |
| Gnomad | rs3819102 |
| Varsome | rs3819102 |
| LitVar | rs3819102 |
| Map | rs3819102 |
| PheGenI | rs3819102 |
| Biobank | rs3819102 |
| 1000 genomes | rs3819102 |
| hgdp | rs3819102 |
| ensembl | rs3819102 |
| geneview | rs3819102 |
| scholar | rs3819102 |
| rs3819102 | |
| pharmgkb | rs3819102 |
| gwascentral | rs3819102 |
| openSNP | rs3819102 |
| 23andMe | rs3819102 |
| SNPshot | rs3819102 |
| SNPdbe | rs3819102 |
| MSV3d | rs3819102 |
| GWAS Ctlg | rs3819102 |
| GMAF | 0.0877 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19190136
] rs3819102 associated with risk of endometrial cancer. The odds ratio (95% confidence interval) for the CC genotype was 1.5 (1.0-2.2) compared with the TT genotype
