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rs13306747

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs13306747(C;G)
Make rs13306747(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position12416775
GenePPARG
is asnp
is mentioned by
dbSNPrs13306747
dbSNP (classic)rs13306747
ClinGenrs13306747
ebirs13306747
HLIrs13306747
Exacrs13306747
Gnomadrs13306747
Varsomers13306747
LitVarrs13306747
Maprs13306747
PheGenIrs13306747
Biobankrs13306747
1000 genomesrs13306747
hgdprs13306747
ensemblrs13306747
geneviewrs13306747
scholarrs13306747
googlers13306747
pharmgkbrs13306747
gwascentralrs13306747
openSNPrs13306747
23andMers13306747
SNPshotrs13306747
SNPdbers13306747
MSV3drs13306747
GWAS Ctlgrs13306747
GMAF0.009642
Max Magnitude0
? (C;C) (C;G) (G;G) 28


[PMID 23907334OA-icon.png] Genetic Variants of Peroxisome Proliferator-Activated Receptor δ Are Associated with Gastric Cancer


[PMID 20416077OA-icon.png] Identification of type 2 diabetes-associated combination of SNPs using support vector machine.


ClinVar
Risk rs13306747(A;A) rs13306747(G;G) rs13306747(T;T)
Alt rs13306747(A;A) rs13306747(G;G) rs13306747(T;T)
Reference Rs13306747(C;C)
Significance Probable-non-pathogenic
Disease Familial partial lipodystrophy Diabetes Mellitus Obesity
Variation info
Gene PPARG
CLNDBN Familial partial lipodystrophy Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension Obesity
Reversed 0
HGVS NC_000003.11:g.12458274C>G
CLNSRC
CLNACC RCV000306988.1, RCV000341948.1, RCV000407637.1,