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rs4907792

From SNPedia

Orientationplus
Stabilizedplus
Make rs4907792(C;C)
Make rs4907792(C;T)
Make rs4907792(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position51505931
GeneLOC102723426
is asnp
is mentioned by
dbSNPrs4907792
ebirs4907792
HLIrs4907792
Exacrs4907792
Varsomers4907792
Maprs4907792
PheGenIrs4907792
hapmaprs4907792
1000 genomesrs4907792
hgdprs4907792
ensemblrs4907792
gopubmedrs4907792
geneviewrs4907792
scholarrs4907792
googlers4907792
pharmgkbrs4907792
gwascentralrs4907792
openSNPrs4907792
23andMers4907792
23andMe allrs4907792
SNP Nexus

SNPshotrs4907792
SNPdbers4907792
MSV3drs4907792
GWAS Ctlgrs4907792
GMAF0.2594
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 24497837OA-icon.png] Comprehensive functional annotation of 77 prostate cancer risk Loci