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rs998124

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs998124(A;G)
Make rs998124(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position45145697
GeneLOC105372091
is asnp
is mentioned by
dbSNPrs998124
dbSNP (classic)rs998124
ClinGenrs998124
ebirs998124
HLIrs998124
Exacrs998124
Gnomadrs998124
Varsomers998124
LitVarrs998124
Maprs998124
PheGenIrs998124
Biobankrs998124
1000 genomesrs998124
hgdprs998124
ensemblrs998124
geneviewrs998124
scholarrs998124
googlers998124
pharmgkbrs998124
gwascentralrs998124
openSNPrs998124
23andMers998124
SNPshotrs998124
SNPdbers998124
MSV3drs998124
GWAS Ctlgrs998124
GMAF0.1065
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 0.000005
Odds Ratio 1.3300 None