Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3812316
rs3812316
Entrez Id: 51085
Gene Symbol: MLXIPL
MLXIPL
CUI: C0010068
Disease:
Coronary heart disease
0.010 GeneticVariation BEFREE C771G (His241Gln) polymorphism of MLXIPL gene, TG levels and coronary artery disease: a case control study. 25179879 2015