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: rs527409
rs527409
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0026691
Disease:
Mucocutaneous Lymph Node Syndrome 		T 0.810 GeneticVariation GWASDB 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: 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: rs527409
rs527409
Entrez Id: 1600
Gene Symbol: DAB1
DAB1
CUI: C0026691
Disease:
Mucocutaneous Lymph Node Syndrome 		T 0.810 GeneticVariation GWASCAT 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: 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: 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: 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: 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: 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: 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: 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: 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: 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