rs10124837
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10124837(C;C) |
| Make rs10124837(C;T) |
| Make rs10124837(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 9 |
| Position | 16891649 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10124837 |
| dbSNP (classic) | rs10124837 |
| ClinGen | rs10124837 |
| ebi | rs10124837 |
| HLI | rs10124837 |
| Exac | rs10124837 |
| Gnomad | rs10124837 |
| Varsome | rs10124837 |
| LitVar | rs10124837 |
| Map | rs10124837 |
| PheGenI | rs10124837 |
| Biobank | rs10124837 |
| 1000 genomes | rs10124837 |
| hgdp | rs10124837 |
| ensembl | rs10124837 |
| geneview | rs10124837 |
| scholar | rs10124837 |
| rs10124837 | |
| pharmgkb | rs10124837 |
| gwascentral | rs10124837 |
| openSNP | rs10124837 |
| 23andMe | rs10124837 |
| SNPshot | rs10124837 |
| SNPdbe | rs10124837 |
| MSV3d | rs10124837 |
| GWAS Ctlg | rs10124837 |
| Max Magnitude | 0 |
[PMID 27463617
] Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
