Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800206
rs1800206
Entrez Id: 5465
Gene Symbol: PPARA
PPARA
CUI: C0020474
Disease:
Hyperlipidemia, Familial Combined
0.010 GeneticVariation BEFREE The frequency of the L162V variant was less in FCHL probands (1.98%) compared to that in spouses (4.84%). 12468272 2002