rs11887120
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11887120(C;C) |
| Make rs11887120(C;T) |
| Make rs11887120(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 25262866 |
| Gene | DNMT3A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11887120 |
| dbSNP (classic) | rs11887120 |
| ClinGen | rs11887120 |
| ebi | rs11887120 |
| HLI | rs11887120 |
| Exac | rs11887120 |
| Gnomad | rs11887120 |
| Varsome | rs11887120 |
| LitVar | rs11887120 |
| Map | rs11887120 |
| PheGenI | rs11887120 |
| Biobank | rs11887120 |
| 1000 genomes | rs11887120 |
| hgdp | rs11887120 |
| ensembl | rs11887120 |
| geneview | rs11887120 |
| scholar | rs11887120 |
| rs11887120 | |
| pharmgkb | rs11887120 |
| gwascentral | rs11887120 |
| openSNP | rs11887120 |
| 23andMe | rs11887120 |
| SNPshot | rs11887120 |
| SNPdbe | rs11887120 |
| MSV3d | rs11887120 |
| GWAS Ctlg | rs11887120 |
| GMAF | 0.4752 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18381459
] 829 Caucasian cases with primary epithelial ovarian cancer and 941 frequency-matched unaffected controls
Three SNPs in DNMT3A were associated with risk among multivitamin supplement users:
- 3' untranslated region (UTR) C>G (rs13420827: OR, 0.8; 95% CI, 0.6-1.0; P interaction = 0.006; FPRP = 0.54)
- intron 6 G>A (rs11887120: OR, 0.8; 95% CI, 0.7-1.0; P interaction = 0.007; FPRP = 0.57)
- intron 22 A>T (rs11695471: OR, 1.2; 95% CI, 1.0-1.5; P interaction = 0.01; FPRP = 0.66)
