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: rs527409
rs527409
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0026691
Disease:
Mucocutaneous Lymph Node Syndrome
0.810 GeneticVariation BEFREE Of these, one locus on chromosome 1p31 (rs527409) was replicated in 266 children with KD and 600 normal controls (odds ratio [OR] = 2.90, 95% confidence interval [CI] = 1.85-4.54, P (combined) = 1.46 × 10(-6)); and a PELI1 locus on chromosome 2p13.3 (rs7604693) was replicated in 86 KD patients with CALs and 600 controls (OR = 2.70, 95% CI = 1.77-4.12, P (combined) = 2.00 × 10(-6)). 21221998 2011
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
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: rs1077424
rs1077424
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0007131
Disease:
Non-Small Cell Lung Carcinoma
0.700 GeneticVariation GWASDB The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations. 21866343 2012
dbSNP: rs11207010
rs11207010
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0007131
Disease:
Non-Small Cell Lung Carcinoma
0.700 GeneticVariation GWASDB The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations. 21866343 2012
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: rs12037261
rs12037261
Entrez Id: 1600;105378746
Gene Symbol: DAB1;LOC105378746
DAB1;LOC105378746
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis
0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs12037261
rs12037261
Entrez Id: 1600;105378746
Gene Symbol: DAB1;LOC105378746
DAB1;LOC105378746
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs12061812
rs12061812
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0007131
Disease:
Non-Small Cell Lung Carcinoma
0.700 GeneticVariation GWASDB The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations. 21866343 2012
dbSNP: rs12086988
rs12086988
Entrez Id: 1600;115209;107984960
Gene Symbol: DAB1;OMA1;LOC107984960
DAB1;OMA1;LOC107984960
CUI: C0200635
Disease:
Lymphocyte Count measurement
0.700 GeneticVariation GWASDB The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes. 22286170 2012
dbSNP: rs12087888
rs12087888
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0007131
Disease:
Non-Small Cell Lung Carcinoma
0.700 GeneticVariation GWASDB The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations. 21866343 2012
dbSNP: rs17425189
rs17425189
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0007131
Disease:
Non-Small Cell Lung Carcinoma
0.700 GeneticVariation GWASDB The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations. 21866343 2012
dbSNP: rs267650
rs267650
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0007131
Disease:
Non-Small Cell Lung Carcinoma
0.700 GeneticVariation GWASDB The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations. 21866343 2012
dbSNP: rs3754260
rs3754260
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs3754260
rs3754260
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis
0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs3909556
rs3909556
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0007131
Disease:
Non-Small Cell Lung Carcinoma
0.700 GeneticVariation GWASDB The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations. 21866343 2012
dbSNP: rs4912182
rs4912182
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs4912182
rs4912182
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis
0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs76484449
rs76484449
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1202773
rs1202773
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0004352
Disease:
Autistic Disorder
0.010 GeneticVariation BEFREE In the total 427 trios, we found significant genetic association between autism and four SNPs in DAB1 (rs12035887 G: p=0.0006; rs3738556 G: p=0.0044; rs1202773 A: p=0.0048; rs12740765 T: p=0.0196). 23333377 2013
dbSNP: rs12035887
rs12035887
Entrez Id: 1600;112267900
Gene Symbol: DAB1;LOC112267900
DAB1;LOC112267900
CUI: C0004352
Disease:
Autistic Disorder
0.010 GeneticVariation BEFREE In the total 427 trios, we found significant genetic association between autism and four SNPs in DAB1 (rs12035887 G: p=0.0006; rs3738556 G: p=0.0044; rs1202773 A: p=0.0048; rs12740765 T: p=0.0196). 23333377 2013
dbSNP: rs12740765
rs12740765
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0004352
Disease:
Autistic Disorder
0.010 GeneticVariation BEFREE In the total 427 trios, we found significant genetic association between autism and four SNPs in DAB1 (rs12035887 G: p=0.0006; rs3738556 G: p=0.0044; rs1202773 A: p=0.0048; rs12740765 T: p=0.0196). 23333377 2013
dbSNP: rs3738556
rs3738556
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0004352
Disease:
Autistic Disorder
0.010 GeneticVariation BEFREE In the total 427 trios, we found significant genetic association between autism and four SNPs in DAB1 (rs12035887 G: p=0.0006; rs3738556 G: p=0.0044; rs1202773 A: p=0.0048; rs12740765 T: p=0.0196). 23333377 2013
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: 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