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rs10277209

From SNPedia

Orientationplus
Stabilizedplus
Make rs10277209(C;C)
Make rs10277209(C;T)
Make rs10277209(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position109363517
is asnp
is mentioned by
dbSNPrs10277209
ebirs10277209
HLIrs10277209
Exacrs10277209
Varsomers10277209
Maprs10277209
PheGenIrs10277209
hapmaprs10277209
1000 genomesrs10277209
hgdprs10277209
ensemblrs10277209
gopubmedrs10277209
geneviewrs10277209
scholarrs10277209
googlers10277209
pharmgkbrs10277209
gwascentralrs10277209
openSNPrs10277209
23andMers10277209
23andMe allrs10277209
SNP Nexus

SNPshotrs10277209
SNPdbers10277209
MSV3drs10277209
GWAS Ctlgrs10277209
GMAF0.152
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22219177OA-icon.png]
Trait
Title A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variants.
Risk Allele
P-val 0.000004
Odds Ratio 1.3600 None