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rs7172432

From SNPedia

Orientationplus
Stabilizedplus
Make rs7172432(A;A)
Make rs7172432(A;G)
Make rs7172432(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position62104190
is asnp
is mentioned by
dbSNPrs7172432
ebirs7172432
HLIrs7172432
Exacrs7172432
Varsomers7172432
Maprs7172432
PheGenIrs7172432
hapmaprs7172432
1000 genomesrs7172432
hgdprs7172432
ensemblrs7172432
gopubmedrs7172432
geneviewrs7172432
scholarrs7172432
googlers7172432
pharmgkbrs7172432
gwascentralrs7172432
openSNPrs7172432
23andMers7172432
23andMe allrs7172432
SNP Nexus

SNPshotrs7172432
SNPdbers7172432
MSV3drs7172432
GWAS Ctlgrs7172432
GMAF0.4972
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20818381]
Trait
Title A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B
Risk Allele
P-val 9E-14
Odds Ratio 1.11 [1.08-1.14]


[PMID 21249489] The diabetogenic VPS13C/C2CD4A/C2CD4B rs7172432 variant impairs glucose-stimulated insulin response in 5,722 non-diabetic Danish individuals

GWAS snp
PMID [PMID 23945395]
Trait Type 2 diabetes
Title Genome-wide association study identifies three novel loci for type 2 diabetes.
Risk Allele A
P-val 1E-6
Odds Ratio 1.11 [1.07-1.16]