rs10761581
From SNPedia
Orientation | minus |
Stabilized | plus |
Make rs10761581(G;G) |
Make rs10761581(G;T) |
Make rs10761581(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 46027444 |
Gene | NCOA4 |
is a | snp |
is | mentioned by |
dbSNP | rs10761581 |
dbSNP (classic) | rs10761581 |
ClinGen | rs10761581 |
ebi | rs10761581 |
HLI | rs10761581 |
Exac | rs10761581 |
Gnomad | rs10761581 |
Varsome | rs10761581 |
LitVar | rs10761581 |
Map | rs10761581 |
PheGenI | rs10761581 |
Biobank | rs10761581 |
1000 genomes | rs10761581 |
hgdp | rs10761581 |
ensembl | rs10761581 |
geneview | rs10761581 |
scholar | rs10761581 |
rs10761581 | |
pharmgkb | rs10761581 |
gwascentral | rs10761581 |
openSNP | rs10761581 |
23andMe | rs10761581 |
SNPshot | rs10761581 |
SNPdbe | rs10761581 |
MSV3d | rs10761581 |
GWAS Ctlg | rs10761581 |
GMAF | 0.41 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
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[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.