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rs10761581

From SNPedia

Orientationminus
Stabilizedplus
Make rs10761581(G;G)
Make rs10761581(G;T)
Make rs10761581(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position46027444
GeneNCOA4
is asnp
is mentioned by
dbSNPrs10761581
dbSNP (classic)rs10761581
ClinGenrs10761581
ebirs10761581
HLIrs10761581
Exacrs10761581
Gnomadrs10761581
Varsomers10761581
LitVarrs10761581
Maprs10761581
PheGenIrs10761581
Biobankrs10761581
1000 genomesrs10761581
hgdprs10761581
ensemblrs10761581
geneviewrs10761581
scholarrs10761581
googlers10761581
pharmgkbrs10761581
gwascentralrs10761581
openSNPrs10761581
23andMers10761581
SNPshotrs10761581
SNPdbers10761581
MSV3drs10761581
GWAS Ctlgrs10761581
GMAF0.41
Max Magnitude0
? (G;G) (G;T) (T;T) 28


[PMID 20717903OA-icon.png] 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 19153072OA-icon.png] Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk.


[PMID 19644707OA-icon.png] Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer.