APOB, apolipoprotein B, 338

N. diseases: 339; N. variants: 122
Disease: Familial hypobetalipoproteinemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553385404
rs1553385404
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C1862596
Disease:
Familial hypobetalipoproteinemia 		T 0.700 CausalMutation CLINVAR