rs7904463
From SNPedia
| Orientation | minus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs7904463(C;T) |
| Make rs7904463(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 46036353 |
| Gene | MSMB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7904463 |
| dbSNP (classic) | rs7904463 |
| ClinGen | rs7904463 |
| ebi | rs7904463 |
| HLI | rs7904463 |
| Exac | rs7904463 |
| Gnomad | rs7904463 |
| Varsome | rs7904463 |
| LitVar | rs7904463 |
| Map | rs7904463 |
| PheGenI | rs7904463 |
| Biobank | rs7904463 |
| 1000 genomes | rs7904463 |
| hgdp | rs7904463 |
| ensembl | rs7904463 |
| geneview | rs7904463 |
| scholar | rs7904463 |
| rs7904463 | |
| pharmgkb | rs7904463 |
| gwascentral | rs7904463 |
| openSNP | rs7904463 |
| 23andMe | rs7904463 |
| SNPshot | rs7904463 |
| SNPdbe | rs7904463 |
| MSV3d | rs7904463 |
| GWAS Ctlg | rs7904463 |
| GMAF | 0.4109 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20717903
] Evidence for an association between prostate cancer and chromosome 8q24 and 10q11 genetic variants in African American men: The flint men's health study
[PMID 19383797] Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility.
