APOB, apolipoprotein B, 338

N. diseases: 339; N. variants: 122
Disease: Hypercholesterolemia, Familial ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs144467873
rs144467873
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		A 0.700 CausalMutation CLINVAR Child-Parent Familial Hypercholesterolemia Screening in Primary Care. 27783906 2016
dbSNP: rs144467873
rs144467873
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		A 0.700 CausalMutation CLINVAR Common mutations of familial hypercholesterolemia patients in Taiwan: characteristics and implications of migrations from southeast China. 22353362 2012