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rs3755863

From SNPedia

Orientationminus
Stabilizedminus
Make rs3755863(A;A)
Make rs3755863(A;G)
Make rs3755863(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position23813899
GenePPARGC1A
is asnp
is mentioned by
dbSNPrs3755863
ebirs3755863
HLIrs3755863
Exacrs3755863
Varsomers3755863
Maprs3755863
PheGenIrs3755863
hapmaprs3755863
1000 genomesrs3755863
hgdprs3755863
ensemblrs3755863
gopubmedrs3755863
geneviewrs3755863
scholarrs3755863
googlers3755863
pharmgkbrs3755863
gwascentralrs3755863
openSNPrs3755863
23andMers3755863
23andMe allrs3755863
SNP Nexus

SNPshotrs3755863
SNPdbers3755863
MSV3drs3755863
GWAS Ctlgrs3755863
GMAF0.371
Max Magnitude
? (A;A) (A;G) (G;G) 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


[PMID 20125101] Glucose levels and genetic variants across transcriptional pathways: interaction effects with BMI


[PMID 18588668OA-icon.png] Association between PPARGC1A polymorphisms and the occurrence of nonalcoholic fatty liver disease (NAFLD).


[PMID 19133136OA-icon.png] The gene coding for PGC-1alpha modifies age at onset in Huntington's Disease.


[PMID 21211002OA-icon.png] Localization of sequence variations in PGC-1alpha influence their modifying effect in Huntington disease.