rs1800206, PPARA

N. diseases: 35
Disease: Lipodystrophy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Lipodystrophy
CUI: C0023787
Disease: Lipodystrophy
0.010 GeneticVariation BEFREE The rare g allele for L162V was found in 15% of patients free of any sign of lipodystrophy and 8% with at least one sign of lipodystrophy (p=0.04) and the rare t allele for H449H was found in 14% of patients free of any sign of lipodystrophy and 23% of patients with at least one sign of lipodystrophy (p=0.05). 21877956 2012