rs3218698
From SNPedia
| Merged into | rs1799757 |
| Orientation | plus |
| Make rs3218698(-;-) |
| Make rs3218698(-;T) |
| Make rs3218698(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 11 |
| Position | 108279481 |
| Gene | ATM |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3218698 |
| dbSNP (classic) | rs3218698 |
| ClinGen | rs3218698 |
| ebi | rs3218698 |
| HLI | rs3218698 |
| Exac | rs3218698 |
| Gnomad | rs3218698 |
| Varsome | rs3218698 |
| LitVar | rs3218698 |
| Map | rs3218698 |
| PheGenI | rs3218698 |
| Biobank | rs3218698 |
| 1000 genomes | rs3218698 |
| hgdp | rs3218698 |
| ensembl | rs3218698 |
| geneview | rs3218698 |
| scholar | rs3218698 |
| rs3218698 | |
| pharmgkb | rs3218698 |
| gwascentral | rs3218698 |
| openSNP | rs3218698 |
| 23andMe | rs3218698 |
| SNPshot | rs3218698 |
| SNPdbe | rs3218698 |
| MSV3d | rs3218698 |
| GWAS Ctlg | rs3218698 |
| Status | Merged into rs1799757 |
| Max Magnitude | 0 |
[PMID 26974709] Polymorphisms in double strand break repair related genes influence radiosensitivity phenotype in lymphocytes from healthy individuals.
