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rs13073869

From SNPedia

Orientationplus
Stabilizedplus
Make rs13073869(A;A)
Make rs13073869(A;G)
Make rs13073869(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position12312494
GenePPARG
is asnp
is mentioned by
dbSNPrs13073869
dbSNP (classic)rs13073869
ClinGenrs13073869
ebirs13073869
HLIrs13073869
Exacrs13073869
Gnomadrs13073869
Varsomers13073869
LitVarrs13073869
Maprs13073869
PheGenIrs13073869
Biobankrs13073869
1000 genomesrs13073869
hgdprs13073869
ensemblrs13073869
geneviewrs13073869
scholarrs13073869
googlers13073869
pharmgkbrs13073869
gwascentralrs13073869
openSNPrs13073869
23andMers13073869
SNPshotrs13073869
SNPdbers13073869
MSV3drs13073869
GWAS Ctlgrs13073869
GMAF0.2686
Max Magnitude0
? (A;A) (A;G) (G;G) 28


Associated with risk of lung cancer in a Chinese population [PMID 18187557]

[PMID 17213274OA-icon.png] Effects of the type 2 diabetes-associated PPARG P12A polymorphism on progression to diabetes and response to troglitazone.