rs16917302
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16917302(A;A) |
| Make rs16917302(A;C) |
| Make rs16917302(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 62501439 |
| Gene | ZNF365 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16917302 |
| dbSNP (classic) | rs16917302 |
| ClinGen | rs16917302 |
| ebi | rs16917302 |
| HLI | rs16917302 |
| Exac | rs16917302 |
| Gnomad | rs16917302 |
| Varsome | rs16917302 |
| LitVar | rs16917302 |
| Map | rs16917302 |
| PheGenI | rs16917302 |
| Biobank | rs16917302 |
| 1000 genomes | rs16917302 |
| hgdp | rs16917302 |
| ensembl | rs16917302 |
| geneview | rs16917302 |
| scholar | rs16917302 |
| rs16917302 | |
| pharmgkb | rs16917302 |
| gwascentral | rs16917302 |
| openSNP | rs16917302 |
| 23andMe | rs16917302 |
| SNPshot | rs16917302 |
| SNPdbe | rs16917302 |
| MSV3d | rs16917302 |
| GWAS Ctlg | rs16917302 |
| GMAF | 0.2043 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 21060860
] Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer
[PMID 22351618] Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
[PMID 24528085] Breast Cancer Association Studies in a Han Chinese Population using 10 European-ancestry-associated Breast Cancer Susceptibility SNPs
