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rs6712932

From SNPedia

Orientationplus
Stabilizedplus
Make rs6712932(C;C)
Make rs6712932(C;T)
Make rs6712932(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position105221141
is asnp
is mentioned by
dbSNPrs6712932
ebirs6712932
HLIrs6712932
Exacrs6712932
Varsomers6712932
Maprs6712932
PheGenIrs6712932
hapmaprs6712932
1000 genomesrs6712932
hgdprs6712932
ensemblrs6712932
gopubmedrs6712932
geneviewrs6712932
scholarrs6712932
googlers6712932
pharmgkbrs6712932
gwascentralrs6712932
openSNPrs6712932
23andMers6712932
23andMe allrs6712932
SNP Nexus

SNPshotrs6712932
SNPdbers6712932
MSV3drs6712932
GWAS Ctlgrs6712932
GMAF0.2819
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17668382OA-icon.png]
Trait Type 2 diabetes
Title Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium
Risk Allele
P-val 0.0000060000000000000002
Odds Ratio 1.52 [1.27-1.82]



GET Evidence
rs6712932
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.382812
summary