DAB1, DAB adaptor protein 1, 1600

N. diseases: 81; N. variants: 43
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10493251
rs10493251
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C2242456
Disease:
thyroid function 		0.700 GeneticVariation GWASDB A locus on chromosome 1p36 is associated with thyrotropin and thyroid function as identified by genome-wide association study. 20826269 2010
dbSNP: rs11576201
rs11576201
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C2242456
Disease:
thyroid function 		0.700 GeneticVariation GWASDB A locus on chromosome 1p36 is associated with thyrotropin and thyroid function as identified by genome-wide association study. 20826269 2010
dbSNP: rs542241509
rs542241509
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0883409
Disease:
Cardiac troponin I measurement 		G 0.700 GeneticVariation GWASCAT Cardiac Troponin T and Troponin I in the General Population. 31014085 2019
dbSNP: rs11207177
rs11207177
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0596887
Disease:
mathematical ability 		T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs1213769
rs1213769
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0596887
Disease:
mathematical ability 		T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs2113453
rs2113453
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0596887
Disease:
mathematical ability 		T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs2185602
rs2185602
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs269051
rs269051
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0596887
Disease:
mathematical ability 		C 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs4620568
rs4620568
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0596887
Disease:
mathematical ability 		C 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs6669975
rs6669975
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0596887
Disease:
mathematical ability 		T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs7537039
rs7537039
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs540431
rs540431
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0424574
Disease:
Duration of sleep 		G 0.700 GeneticVariation GWASCAT Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways. 30804565 2019
dbSNP: rs6679454
rs6679454
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C2699541
Disease:
Cytokine Measurement 		G 0.700 GeneticVariation GWASCAT Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients. 22610502 2012
dbSNP: rs269054
rs269054
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0424574
Disease:
Duration of sleep 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates. 30846698 2019
dbSNP: rs74834332
rs74834332
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C1285654
Disease:
Memory performance 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. 29274321 2018
dbSNP: rs10493240
rs10493240
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10493241
rs10493241
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10493249
rs10493249
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs1213640
rs1213640
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs12726314
rs12726314
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs1475260
rs1475260
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs7546303
rs7546303
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs973236
rs973236
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs17579352
rs17579352
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0948008
Disease:
Ischemic stroke 		C 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke. 26674333 2016
dbSNP: rs852787
rs852787
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C1956346
Disease:
Coronary Artery Disease 		0.710 GeneticVariation BEFREE How rs852787 and its host gene <i>DAB1</i> are linked to CAD needs further studies. 29472232 2018