rs4987945
From SNPedia
| Merged into | rs2227924 |
| Orientation | plus |
| Stabilized | plus |
| Make rs4987945(C;C) |
| Make rs4987945(C;G) |
| Make rs4987945(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 108251865 |
| Gene | ATM |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4987945 |
| dbSNP (classic) | rs4987945 |
| ClinGen | rs4987945 |
| ebi | rs4987945 |
| HLI | rs4987945 |
| Exac | rs4987945 |
| Gnomad | rs4987945 |
| Varsome | rs4987945 |
| LitVar | rs4987945 |
| Map | rs4987945 |
| PheGenI | rs4987945 |
| Biobank | rs4987945 |
| 1000 genomes | rs4987945 |
| hgdp | rs4987945 |
| ensembl | rs4987945 |
| geneview | rs4987945 |
| scholar | rs4987945 |
| rs4987945 | |
| pharmgkb | rs4987945 |
| gwascentral | rs4987945 |
| openSNP | rs4987945 |
| 23andMe | rs4987945 |
| SNPshot | rs4987945 |
| SNPdbe | rs4987945 |
| MSV3d | rs4987945 |
| GWAS Ctlg | rs4987945 |
| Status | Merged into rs2227924 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
This SNP, a variant in the ATM gene, is 1 of 25 SNPs reported to represent independently minor, but cumulatively significant, increased risk for breast cancer. [PMID 17341484]
For details of all 25 SNPs in this group, along with the two methods used to calculate overall risk estimates for breast cancer, refer to the SNPedia breast cancer entry.
For this particular SNP, the risk (minor) allele is (G).
