Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137854499
rs137854499
0.700 GeneticVariation UNIPROT Differential phospholipid substrates and directional transport by ATP-binding cassette proteins ABCA1, ABCA7, and ABCA4 and disease-causing mutants. 24097981

2013

dbSNP: rs145183203
rs145183203
0.700 GeneticVariation UNIPROT Differential phospholipid substrates and directional transport by ATP-binding cassette proteins ABCA1, ABCA7, and ABCA4 and disease-causing mutants. 24097981

2013

dbSNP: rs28933692
rs28933692
0.700 GeneticVariation UNIPROT Differential phospholipid substrates and directional transport by ATP-binding cassette proteins ABCA1, ABCA7, and ABCA4 and disease-causing mutants. 24097981

2013

dbSNP: rs760768125
rs760768125
0.700 GeneticVariation UNIPROT Differential phospholipid substrates and directional transport by ATP-binding cassette proteins ABCA1, ABCA7, and ABCA4 and disease-causing mutants. 24097981

2013

dbSNP: rs137854499
rs137854499
0.700 GeneticVariation UNIPROT Evaluation and treatment of hypertriglyceridemia: an Endocrine Society clinical practice guideline. 22962670

2012

dbSNP: rs28933692
rs28933692
0.700 GeneticVariation UNIPROT Evaluation and treatment of hypertriglyceridemia: an Endocrine Society clinical practice guideline. 22962670

2012

dbSNP: rs137854499
rs137854499
0.700 GeneticVariation UNIPROT Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency. 15722566

2005

dbSNP: rs145183203
rs145183203
0.700 GeneticVariation UNIPROT Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency. 15722566

2005

dbSNP: rs28933692
rs28933692
0.700 GeneticVariation UNIPROT Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency. 15722566

2005

dbSNP: rs760768125
rs760768125
0.700 GeneticVariation UNIPROT Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency. 15722566

2005

dbSNP: rs137854499
rs137854499
0.700 GeneticVariation UNIPROT ABCA1(Alabama): a novel variant associated with HDL deficiency and premature coronary artery disease. 12204794

2002

dbSNP: rs137854499
rs137854499
0.700 GeneticVariation UNIPROT Novel ABCA1 compound variant associated with HDL cholesterol deficiency. 12009425

2002

dbSNP: rs145183203
rs145183203
0.700 GeneticVariation UNIPROT ABCA1(Alabama): a novel variant associated with HDL deficiency and premature coronary artery disease. 12204794

2002

dbSNP: rs145183203
rs145183203
0.700 GeneticVariation UNIPROT Novel ABCA1 compound variant associated with HDL cholesterol deficiency. 12009425

2002

dbSNP: rs28933692
rs28933692
0.700 GeneticVariation UNIPROT ABCA1(Alabama): a novel variant associated with HDL deficiency and premature coronary artery disease. 12204794

2002

dbSNP: rs28933692
rs28933692
0.700 GeneticVariation UNIPROT Novel ABCA1 compound variant associated with HDL cholesterol deficiency. 12009425

2002

dbSNP: rs760768125
rs760768125
0.700 GeneticVariation UNIPROT Novel ABCA1 compound variant associated with HDL cholesterol deficiency. 12009425

2002

dbSNP: rs760768125
rs760768125
0.700 GeneticVariation UNIPROT ABCA1(Alabama): a novel variant associated with HDL deficiency and premature coronary artery disease. 12204794

2002

dbSNP: rs137854499
rs137854499
0.700 GeneticVariation UNIPROT Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes. 11086027

2000

dbSNP: rs145183203
rs145183203
0.700 GeneticVariation UNIPROT Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes. 11086027

2000

dbSNP: rs28933692
rs28933692
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
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
0.700 GeneticVariation UNIPROT Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. 10431236

1999

dbSNP: rs137854499
rs137854499
0.700 GeneticVariation UNIPROT Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. 10533863

1999

dbSNP: rs145183203
rs145183203
0.700 GeneticVariation UNIPROT Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. 10533863

1999