APOB, apolipoprotein B, 338

N. diseases: 339; N. variants: 122
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5742904
rs5742904
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		A 0.800 CausalMutation CLINVAR
dbSNP: rs1057518647
rs1057518647
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020597
Disease:
Hypobetalipoproteinemias 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518647
rs1057518647
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C4551990
Disease:
Acanthocytosis With Hypobetalipoproteinemia 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1060499841
rs1060499841
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1135402762
rs1135402762
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1135402764
rs1135402764
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1135402765
rs1135402765
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1135402766
rs1135402766
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		G 0.700 CausalMutation CLINVAR
dbSNP: rs121918383
rs121918383
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C1862596
Disease:
Familial hypobetalipoproteinemia 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121918384
rs121918384
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C1862596
Disease:
Familial hypobetalipoproteinemia 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121918385
rs121918385
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C1862596
Disease:
Familial hypobetalipoproteinemia 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121918386
rs121918386
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C1862596
Disease:
Familial hypobetalipoproteinemia 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121918387
rs121918387
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C1862596
Disease:
Familial hypobetalipoproteinemia 		C 0.700 CausalMutation CLINVAR
dbSNP: rs121918388
rs121918388
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C4551990
Disease:
Acanthocytosis With Hypobetalipoproteinemia 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121918389
rs121918389
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C1862596
Disease:
Familial hypobetalipoproteinemia 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121918390
rs121918390
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C1862596
Disease:
Familial hypobetalipoproteinemia 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121918391
rs121918391
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C4551990
Disease:
Acanthocytosis With Hypobetalipoproteinemia 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1339117465
rs1339117465
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1382988295
rs1382988295
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1382988295
rs1382988295
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1399892057
rs1399892057
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C4551990
Disease:
Acanthocytosis With Hypobetalipoproteinemia 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1418775778
rs1418775778
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		T 0.700 CausalMutation CLINVAR
dbSNP: rs142017360
rs142017360
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1442815965
rs1442815965
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		A 0.700 CausalMutation CLINVAR
dbSNP: rs146377316
rs146377316
Entrez Id: 338
Gene Symbol: APOB
APOB
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		A 0.700 CausalMutation CLINVAR