PPARGC1A, PPARG coactivator 1 alpha, 10891

N. diseases: 350; N. variants: 42
Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8192678
rs8192678
Entrez Id: 10891
Gene Symbol: PPARGC1A
PPARGC1A
CUI: C0030567
Disease:
Parkinson Disease 		0.020 GeneticVariation BEFREE We estimate statistical interactions between MB/PQ and PPARGC1α rs6821591 (interaction p = 0.009) and rs8192678 (interaction p = 0.05), such that those with high exposure and the variant allele were at an increased risk of PD (OR ≥ 1.30, p ≤ 0.05). 29630901 2018
dbSNP: rs8192678
rs8192678
Entrez Id: 10891
Gene Symbol: PPARGC1A
PPARGC1A
CUI: C0030567
Disease:
Parkinson Disease 		0.020 GeneticVariation BEFREE The rs8192678 PGC-1α SNP was not associated with the risk of PD. 21595954 2011