Rs10761581
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10761581 |
| PheGenI | rs10761581 |
| nextbio | rs10761581 |
| hapmap | rs10761581 |
| 1000 genomes | rs10761581 |
| hgdp | rs10761581 |
| ensembl | rs10761581 |
| gopubmed | rs10761581 |
| geneview | rs10761581 |
| scholar | rs10761581 |
| rs10761581 | |
| pharmgkb | rs10761581 |
| gwascentral | rs10761581 |
| openSNP | rs10761581 |
| 23andMe | rs10761581 |
| 23andMe all | rs10761581 |
| SNP Nexus | |
| SNPshot | rs10761581 |
| SNPdbe | rs10761581 |
| MSV3d | rs10761581 |
| Gene | NCOA4, TIMM23B |
| Chromosome | 10 |
| Orientation | plus |
| GMAF | 0.4098 |
| Position | 51568378 |
| Reference | GRCh37.p2 37.2/134 |
| Max Magnitude |
| Make rs10761581(G;G) |
| Make rs10761581(G;T) |
| Make rs10761581(T;T) |
| ? | (G;G) (G;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 19153072] Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk.
[PMID 19644707] Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer.
| GET Evidence | |
|---|---|
| NCOA4-F8V | |
| aa_change | Phe8Val |
| aa_change_short | F8V |
| impact | not reviewed |
| qualified_impact | Insufficiently evaluated not reviewed |
| overall_frequency | 0.422387 |
| summary | |
