rs3816659
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3816659(C;C) |
| Make rs3816659(C;T) |
| Make rs3816659(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 1317705 |
| Gene | CLPTM1L |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3816659 |
| dbSNP (classic) | rs3816659 |
| ClinGen | rs3816659 |
| ebi | rs3816659 |
| HLI | rs3816659 |
| Exac | rs3816659 |
| Gnomad | rs3816659 |
| Varsome | rs3816659 |
| LitVar | rs3816659 |
| Map | rs3816659 |
| PheGenI | rs3816659 |
| Biobank | rs3816659 |
| 1000 genomes | rs3816659 |
| hgdp | rs3816659 |
| ensembl | rs3816659 |
| geneview | rs3816659 |
| scholar | rs3816659 |
| rs3816659 | |
| pharmgkb | rs3816659 |
| gwascentral | rs3816659 |
| openSNP | rs3816659 |
| 23andMe | rs3816659 |
| SNPshot | rs3816659 |
| SNPdbe | rs3816659 |
| MSV3d | rs3816659 |
| GWAS Ctlg | rs3816659 |
| GMAF | 0.3572 |
| Max Magnitude | 0 |
[PMID 20056641
] Multiple genetic variants in telomere pathway genes and breast cancer risk
