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rs7904463

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs7904463(C;T)
Make rs7904463(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position46036353
GeneMSMB, TIMM23B
is asnp
is mentioned by
dbSNPrs7904463
ebirs7904463
HLIrs7904463
Exacrs7904463
Varsomers7904463
Maprs7904463
PheGenIrs7904463
hapmaprs7904463
1000 genomesrs7904463
hgdprs7904463
ensemblrs7904463
gopubmedrs7904463
geneviewrs7904463
scholarrs7904463
googlers7904463
pharmgkbrs7904463
gwascentralrs7904463
openSNPrs7904463
23andMers7904463
23andMe allrs7904463
SNP Nexus

SNPshotrs7904463
SNPdbers7904463
MSV3drs7904463
GWAS Ctlgrs7904463
GMAF0.4109
Max Magnitude0
? (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 19383797OA-icon.png] Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility.