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rs2029167

From SNPedia

Orientationplus
Stabilizedplus
Make rs2029167(A;A)
Make rs2029167(A;G)
Make rs2029167(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position54196349
is asnp
is mentioned by
dbSNPrs2029167
ebirs2029167
HLIrs2029167
Exacrs2029167
Varsomers2029167
Maprs2029167
PheGenIrs2029167
hapmaprs2029167
1000 genomesrs2029167
hgdprs2029167
ensemblrs2029167
gopubmedrs2029167
geneviewrs2029167
scholarrs2029167
googlers2029167
pharmgkbrs2029167
gwascentralrs2029167
openSNPrs2029167
23andMers2029167
23andMe allrs2029167
SNP Nexus

SNPshotrs2029167
SNPdbers2029167
MSV3drs2029167
GWAS Ctlgrs2029167
GMAF0.4853
Max Magnitude

[PMID 24038406] Genetic variations in base excision repair pathway and risk of bladder cancer: A case-control study in the United States