Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs752100893
rs752100893
Entrez Id: 4547
Gene Symbol: MTTP
MTTP
CUI: C0542037
Disease:
Hypotriglyceridemia
0.010 GeneticVariation BEFREE Functional analysis of the missense APOC3 mutation Ala23Thr associated with human hypotriglyceridemia. 20097930 2010