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rs12155172

From SNPedia

Orientationplus
Stabilizedplus
Make rs12155172(A;A)
Make rs12155172(A;G)
Make rs12155172(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position20954872
is asnp
is mentioned by
dbSNPrs12155172
ebirs12155172
HLIrs12155172
Exacrs12155172
Varsomers12155172
Maprs12155172
PheGenIrs12155172
hapmaprs12155172
1000 genomesrs12155172
hgdprs12155172
ensemblrs12155172
gopubmedrs12155172
geneviewrs12155172
scholarrs12155172
googlers12155172
pharmgkbrs12155172
gwascentralrs12155172
openSNPrs12155172
23andMers12155172
23andMe allrs12155172
SNP Nexus

SNPshotrs12155172
SNPdbers12155172
MSV3drs12155172
GWAS Ctlgrs12155172
GMAF0.1855
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19767753OA-icon.png]
Trait Prostate cancer
Title Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
Risk Allele A
P-val 0.000009
Odds Ratio 1.05 [1.00-1.10]


GET Evidence
rs12155172
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.757812
summary



GWAS snp
PMID [PMID 23535732OA-icon.png]
Trait Prostate cancer
Title Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.
Risk Allele A
P-val 5E-13
Odds Ratio 1.11 [1.07-1.15]