DOCK3, dedicator of cytokinesis 3, 1795

N. diseases: 85; N. variants: 51
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10510757
rs10510757
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs13069365
rs13069365
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C0424621
Disease:
Body Fat Distribution 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects. 30664634 2019
dbSNP: rs142515812
rs142515812
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C4749014
Disease:
NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA 		0.700 GeneticVariation UNIPROT Variants in DOCK3 cause developmental delay and hypotonia. 30976111 2019
dbSNP: rs199600118
rs199600118
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C4749014
Disease:
NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA 		0.700 GeneticVariation UNIPROT Variants in DOCK3 cause developmental delay and hypotonia. 30976111 2019
dbSNP: rs201184598
rs201184598
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C4749014
Disease:
NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA 		0.700 GeneticVariation UNIPROT Variants in DOCK3 cause developmental delay and hypotonia. 30976111 2019
dbSNP: rs62257807
rs62257807
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C0017654
Disease:
Glomerular Filtration Rate 		T 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs73072483
rs73072483
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11920441
rs11920441
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C4317009
Disease:
Diverticular Diseases 		C 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify 39 new susceptibility loci for diverticular disease. 30177863 2018
dbSNP: rs142515812
rs142515812
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C4749014
Disease:
NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA 		0.700 GeneticVariation UNIPROT DOCK3-related neurodevelopmental syndrome: Biallelic intragenic deletion of DOCK3 in a boy with developmental delay and hypotonia. 29130632 2018
dbSNP: rs1552074
rs1552074
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs1553749681
rs1553749681
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 GeneticVariation CLINVAR DOCK3-related neurodevelopmental syndrome: Biallelic intragenic deletion of DOCK3 in a boy with developmental delay and hypotonia. 29130632 2018
dbSNP: rs1553749681
rs1553749681
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C0432072
Disease:
Dysmorphic features 		T 0.700 GeneticVariation CLINVAR DOCK3-related neurodevelopmental syndrome: Biallelic intragenic deletion of DOCK3 in a boy with developmental delay and hypotonia. 29130632 2018
dbSNP: rs1553749681
rs1553749681
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C0026650
Disease:
Movement Disorders 		T 0.700 GeneticVariation CLINVAR DOCK3-related neurodevelopmental syndrome: Biallelic intragenic deletion of DOCK3 in a boy with developmental delay and hypotonia. 29130632 2018
dbSNP: rs199600118
rs199600118
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C4749014
Disease:
NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA 		0.700 GeneticVariation UNIPROT DOCK3-related neurodevelopmental syndrome: Biallelic intragenic deletion of DOCK3 in a boy with developmental delay and hypotonia. 29130632 2018
dbSNP: rs201184598
rs201184598
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C4749014
Disease:
NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA 		0.700 GeneticVariation UNIPROT DOCK3-related neurodevelopmental syndrome: Biallelic intragenic deletion of DOCK3 in a boy with developmental delay and hypotonia. 29130632 2018
dbSNP: rs7633959
rs7633959
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
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: rs10510754
rs10510754
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
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: rs11130263
rs11130263
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
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: rs11917538
rs11917538
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
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: rs11921930
rs11921930
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
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: rs142515812
rs142515812
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C4749014
Disease:
NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA 		0.700 GeneticVariation UNIPROT Biallelic loss-of-function variants in DOCK3 cause muscle hypotonia, ataxia, and intellectual disability. 28195318 2017
dbSNP: rs1553749681
rs1553749681
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C0432072
Disease:
Dysmorphic features 		T 0.700 GeneticVariation CLINVAR Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome. 28139846 2017
dbSNP: rs1553749681
rs1553749681
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 GeneticVariation CLINVAR Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome. 28139846 2017
dbSNP: rs1553749681
rs1553749681
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C0432072
Disease:
Dysmorphic features 		T 0.700 GeneticVariation CLINVAR Biallelic loss-of-function variants in DOCK3 cause muscle hypotonia, ataxia, and intellectual disability. 28195318 2017
dbSNP: rs1553749681
rs1553749681
Entrez Id: 1795
Gene Symbol: DOCK3
DOCK3
CUI: C0026650
Disease:
Movement Disorders 		T 0.700 GeneticVariation CLINVAR Biallelic loss-of-function variants in DOCK3 cause muscle hypotonia, ataxia, and intellectual disability. 28195318 2017