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rs2270031

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2270031(C;G)
Make rs2270031(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position1633343
GeneWNT5B
is asnp
is mentioned by
dbSNPrs2270031
ebirs2270031
HLIrs2270031
Exacrs2270031
Varsomers2270031
Maprs2270031
PheGenIrs2270031
hapmaprs2270031
1000 genomesrs2270031
hgdprs2270031
ensemblrs2270031
gopubmedrs2270031
geneviewrs2270031
scholarrs2270031
googlers2270031
pharmgkbrs2270031
gwascentralrs2270031
openSNPrs2270031
23andMers2270031
23andMe allrs2270031
SNP Nexus

SNPshotrs2270031
SNPdbers2270031
MSV3drs2270031
GWAS Ctlgrs2270031
GMAF0.1295
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 18555673] IVS3C>G variant (rs2270031) may influence type-2 diabetes