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rs1016342

From SNPedia

Orientationplus
Stabilizedplus
Make rs1016342(C;C)
Make rs1016342(C;T)
Make rs1016342(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position127080210
GenePRNCR1
is asnp
is mentioned by
dbSNPrs1016342
ebirs1016342
HLIrs1016342
Exacrs1016342
Varsomers1016342
Maprs1016342
PheGenIrs1016342
hapmaprs1016342
1000 genomesrs1016342
hgdprs1016342
ensemblrs1016342
gopubmedrs1016342
geneviewrs1016342
scholarrs1016342
googlers1016342
pharmgkbrs1016342
gwascentralrs1016342
openSNPrs1016342
23andMers1016342
23andMe allrs1016342
SNP Nexus

SNPshotrs1016342
SNPdbers1016342
MSV3drs1016342
GWAS Ctlgrs1016342
GMAF0.4614
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19562729OA-icon.png] Common variants in 8q24 are associated with risk for prostate cancer and tumor aggressiveness in men of European ancestry