rs150599989, C5AR2

N. diseases: 5
Disease: Hyperlipidemia, Familial Combined ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
0.020 GeneticVariation BEFREE We found no evidence to demonstrate that the S323I polymorphism contributes to familial combined hyperlipidemia or type 2 diabetes in the Chinese population. 22194190 2011
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
0.020 GeneticVariation BEFREE The S323I variant may alter C5L2 function and might be one molecular basis contributing to familial combined hyperlipidemia. 16627811 2006