Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs150599989
rs150599989
C5AR2
0.010 GeneticVariation BEFREE Identification of a novel C5L2 variant (S323I) in a French Canadian family with familial combined hyperlipemia. 16627811

2006