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rs4489787

From SNPedia

Orientationplus
Stabilizedplus
Make rs4489787(C;C)
Make rs4489787(C;T)
Make rs4489787(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position48417317
GeneLOC102723866
is asnp
is mentioned by
dbSNPrs4489787
ebirs4489787
HLIrs4489787
Exacrs4489787
Varsomers4489787
Maprs4489787
PheGenIrs4489787
hapmaprs4489787
1000 genomesrs4489787
hgdprs4489787
ensemblrs4489787
gopubmedrs4489787
geneviewrs4489787
scholarrs4489787
googlers4489787
pharmgkbrs4489787
gwascentralrs4489787
openSNPrs4489787
23andMers4489787
23andMe allrs4489787
SNP Nexus

SNPshotrs4489787
SNPdbers4489787
MSV3drs4489787
GWAS Ctlgrs4489787
GMAF0.07346
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 0.000001
Odds Ratio 1.4700 None