Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2187331
rs2187331
LOC107984343
0.010 GeneticVariation BEFREE The SNP rs2187331 is associated with HTG in FCHL and white combined hyperlipidemia cases/controls and influences TG levels in the population. 18988886

2009
dbSNP: rs1805087
rs1805087
MTR
0.010 GeneticVariation BEFREE HHcy and MS A2756G mutation may be the risk factors for combined hyperlipidemia. 19263808

2008
dbSNP: rs1801282
rs1801282
PPARG
0.010 GeneticVariation BEFREE Obese carriers of the Pro12Ala polymorphism have a greater risk of developing combined hyperlipidaemia, possibly due to impaired activation of PPAR gamma target genes. 11248748

2001
dbSNP: rs1805192
rs1805192
PPARG
0.010 GeneticVariation BEFREE Obese carriers of the Pro12Ala polymorphism have a greater risk of developing combined hyperlipidaemia, possibly due to impaired activation of PPAR gamma target genes. 11248748

2001