DOCK2, dedicator of cytokinesis 2, 1794

N. diseases: 40; N. variants: 15
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6860963
rs6860963
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs76551843
rs76551843
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
CUI: C0600139
Disease:
Prostate carcinoma 		A 0.700 GeneticVariation GWASCAT Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. 29892016 2018
dbSNP: rs7729471
rs7729471
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
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: rs7729471
rs7729471
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
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: rs13155521
rs13155521
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs262836
rs262836
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
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: rs262860
rs262860
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
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: rs264883
rs264883
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
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: rs4042095
rs4042095
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
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: rs746468
rs746468
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
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: rs90213
rs90213
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
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: rs1561585424
rs1561585424
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
CUI: C4225328
Disease:
IMMUNODEFICIENCY 40 		A 0.700 GeneticVariation CLINVAR Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections. 26083206 2015
dbSNP: rs1561898523
rs1561898523
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
CUI: C4225328
Disease:
IMMUNODEFICIENCY 40 		A 0.700 GeneticVariation CLINVAR Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections. 26083206 2015
dbSNP: rs169082
rs169082
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
CUI: C1295176
Disease:
Leptin measurement 		0.700 GeneticVariation GWASCAT A genome-wide association study identifies protein quantitative trait loci (pQTLs). 18464913 2008
dbSNP: rs762909359
rs762909359
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
CUI: C4225328
Disease:
IMMUNODEFICIENCY 40 		T 0.700 CausalMutation CLINVAR
dbSNP: rs780318765
rs780318765
Entrez Id: 1794
Gene Symbol: DOCK2
DOCK2
CUI: C4225328
Disease:
IMMUNODEFICIENCY 40 		0.700 GeneticVariation UNIPROT