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rs13117172

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs13117172(C;T)
Make rs13117172(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position23878892
GenePPARGC1A
is asnp
is mentioned by
dbSNPrs13117172
ebirs13117172
HLIrs13117172
Exacrs13117172
Varsomers13117172
Maprs13117172
PheGenIrs13117172
hapmaprs13117172
1000 genomesrs13117172
hgdprs13117172
ensemblrs13117172
gopubmedrs13117172
geneviewrs13117172
scholarrs13117172
googlers13117172
pharmgkbrs13117172
gwascentralrs13117172
openSNPrs13117172
23andMers13117172
23andMe allrs13117172
SNP Nexus

SNPshotrs13117172
SNPdbers13117172
MSV3drs13117172
GWAS Ctlgrs13117172
GMAF0.3356
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 19183932] PPARGC1A sequence variation and cardiovascular risk-factor levels: a study of the main genetic effects and gene x environment interactions in children from the European Youth Heart Study