rs228595
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs228595(A;A) |
| Make rs228595(A;G) |
| Make rs228595(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 108234866 |
| Gene | ATM |
| is a | snp |
| is | mentioned by |
| dbSNP | rs228595 |
| dbSNP (classic) | rs228595 |
| ClinGen | rs228595 |
| ebi | rs228595 |
| HLI | rs228595 |
| Exac | rs228595 |
| Gnomad | rs228595 |
| Varsome | rs228595 |
| LitVar | rs228595 |
| Map | rs228595 |
| PheGenI | rs228595 |
| Biobank | rs228595 |
| 1000 genomes | rs228595 |
| hgdp | rs228595 |
| ensembl | rs228595 |
| geneview | rs228595 |
| scholar | rs228595 |
| rs228595 | |
| pharmgkb | rs228595 |
| gwascentral | rs228595 |
| openSNP | rs228595 |
| 23andMe | rs228595 |
| SNPshot | rs228595 |
| SNPdbe | rs228595 |
| MSV3d | rs228595 |
| GWAS Ctlg | rs228595 |
| Max Magnitude | 0 |
[PMID 27796716
] Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.
