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: rs747606537
rs747606537
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		T 0.700 CausalMutation CLINVAR