rs10995201
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10995201(A;A) |
| Make rs10995201(A;G) |
| Make rs10995201(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 10 |
| Position | 62540131 |
| Gene | ZNF365 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10995201 |
| dbSNP (classic) | rs10995201 |
| ClinGen | rs10995201 |
| ebi | rs10995201 |
| HLI | rs10995201 |
| Exac | rs10995201 |
| Gnomad | rs10995201 |
| Varsome | rs10995201 |
| LitVar | rs10995201 |
| Map | rs10995201 |
| PheGenI | rs10995201 |
| Biobank | rs10995201 |
| 1000 genomes | rs10995201 |
| hgdp | rs10995201 |
| ensembl | rs10995201 |
| geneview | rs10995201 |
| scholar | rs10995201 |
| rs10995201 | |
| pharmgkb | rs10995201 |
| gwascentral | rs10995201 |
| openSNP | rs10995201 |
| 23andMe | rs10995201 |
| SNPshot | rs10995201 |
| SNPdbe | rs10995201 |
| MSV3d | rs10995201 |
| GWAS Ctlg | rs10995201 |
| Max Magnitude | 0 |
[PMID 26073781
] Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression
