rs137854499
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Novel ABCA1 compound variant associated with HDL cholesterol deficiency.
|
12009425 |
2002 |
rs137854499
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes.
|
11086027 |
2000 |
rs137854499
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
ABCA1(Alabama): a novel variant associated with HDL deficiency and premature coronary artery disease.
|
12204794 |
2002 |
rs137854499
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency.
|
15722566 |
2005 |
rs137854499
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency.
|
10431236 |
1999 |
rs137854499
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Evaluation and treatment of hypertriglyceridemia: an Endocrine Society clinical practice guideline.
|
22962670 |
2012 |
rs137854499
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux.
|
10533863 |
1999 |
rs137854499
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
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 |
rs145183203
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Novel ABCA1 compound variant associated with HDL cholesterol deficiency.
|
12009425 |
2002 |
rs145183203
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency.
|
10431236 |
1999 |
rs145183203
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency.
|
15722566 |
2005 |
rs145183203
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
ABCA1(Alabama): a novel variant associated with HDL deficiency and premature coronary artery disease.
|
12204794 |
2002 |
rs145183203
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux.
|
10533863 |
1999 |
rs145183203
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
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 |
rs145183203
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes.
|
11086027 |
2000 |
rs28933692
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Novel ABCA1 compound variant associated with HDL cholesterol deficiency.
|
12009425 |
2002 |
rs28933692
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency.
|
15722566 |
2005 |
rs28933692
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
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 |
rs28933692
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux.
|
10533863 |
1999 |
rs28933692
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Evaluation and treatment of hypertriglyceridemia: an Endocrine Society clinical practice guideline.
|
22962670 |
2012 |
rs28933692
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency.
|
10431236 |
1999 |
rs28933692
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
ABCA1(Alabama): a novel variant associated with HDL deficiency and premature coronary artery disease.
|
12204794 |
2002 |
rs28933692
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes.
|
11086027 |
2000 |
rs369098049
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs760507032
|
Entrez Id: |
19 |
Gene Symbol: |
ABCA1 |
ABCA1
|
Hypoalphalipoproteinemia, Familial
|
C |
0.700 |
CausalMutation |
CLINVAR |
Multiple rare alleles contribute to low plasma levels of HDL cholesterol.
|
15297675 |
2004 |