ABCA1, ATP binding cassette subfamily A member 1, 19

N. diseases: 291; N. variants: 116
Disease: Hypoalphalipoproteinemia, Familial ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28933692
rs28933692
Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C1704429
Disease:
Hypoalphalipoproteinemia, Familial 		0.700 GeneticVariation UNIPROT Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes. 11086027 2000
dbSNP: rs760768125
rs760768125
Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C1704429
Disease:
Hypoalphalipoproteinemia, Familial 		0.700 GeneticVariation UNIPROT Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes. 11086027 2000
dbSNP: rs137854499
rs137854499
Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C1704429
Disease:
Hypoalphalipoproteinemia, Familial 		0.700 GeneticVariation UNIPROT Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. 10431236 1999
dbSNP: rs137854499
rs137854499
Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C1704429
Disease:
Hypoalphalipoproteinemia, Familial 		0.700 GeneticVariation UNIPROT Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. 10533863 1999
dbSNP: rs145183203
rs145183203
Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C1704429
Disease:
Hypoalphalipoproteinemia, Familial 		0.700 GeneticVariation UNIPROT Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. 10431236 1999
dbSNP: rs145183203
rs145183203
Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C1704429
Disease:
Hypoalphalipoproteinemia, Familial 		0.700 GeneticVariation UNIPROT Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. 10533863 1999
dbSNP: rs28933692
rs28933692
Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C1704429
Disease:
Hypoalphalipoproteinemia, Familial 		0.700 GeneticVariation UNIPROT Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. 10533863 1999
dbSNP: rs28933692
rs28933692
Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C1704429
Disease:
Hypoalphalipoproteinemia, Familial 		0.700 GeneticVariation UNIPROT Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. 10431236 1999
dbSNP: rs760768125
rs760768125
Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C1704429
Disease:
Hypoalphalipoproteinemia, Familial 		0.700 GeneticVariation UNIPROT Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. 10533863 1999
dbSNP: rs760768125
rs760768125
Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C1704429
Disease:
Hypoalphalipoproteinemia, Familial 		0.700 GeneticVariation UNIPROT Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. 10431236 1999
dbSNP: rs369098049
rs369098049
Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C1704429
Disease:
Hypoalphalipoproteinemia, Familial 		0.700 GeneticVariation UNIPROT