Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113298164
rs113298164
Entrez Id: 3990
Gene Symbol: LIPC
LIPC
CUI: C3151466
Disease:
HEPATIC LIPASE DEFICIENCY (disorder)
T 0.800 CausalMutation CLINVAR
dbSNP: rs113298164
rs113298164
Entrez Id: 3990
Gene Symbol: LIPC
LIPC
CUI: C3151466
Disease:
HEPATIC LIPASE DEFICIENCY (disorder)
0.800 GeneticVariation UNIPROT
dbSNP: rs113298164
rs113298164
Entrez Id: 3990
Gene Symbol: LIPC
LIPC
CUI: C3151466
Disease:
HEPATIC LIPASE DEFICIENCY (disorder)
T 0.800 GeneticVariation CLINVAR