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rs16867225

From SNPedia

Orientationplus
Stabilizedplus
Make rs16867225(A;A)
Make rs16867225(A;G)
Make rs16867225(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position180176559
is asnp
is mentioned by
dbSNPrs16867225
dbSNP (classic)rs16867225
ClinGenrs16867225
ebirs16867225
HLIrs16867225
Exacrs16867225
Gnomadrs16867225
Varsomers16867225
LitVarrs16867225
Maprs16867225
PheGenIrs16867225
Biobankrs16867225
1000 genomesrs16867225
hgdprs16867225
ensemblrs16867225
geneviewrs16867225
scholarrs16867225
googlers16867225
pharmgkbrs16867225
gwascentralrs16867225
openSNPrs16867225
23andMers16867225
SNPshotrs16867225
SNPdbers16867225
MSV3drs16867225
GWAS Ctlgrs16867225
GMAF0.1901
Max Magnitude0
? (A;A) (A;G) (G;G) 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 0.000003
Odds Ratio 1.5625 None