Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs112193369
rs112193369
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0600139
Disease:
Prostate carcinoma
0.700 GeneticVariation GWASCAT Radiogenomics Consortium Genome-Wide Association Study Meta-Analysis of Late Toxicity After Prostate Cancer Radiotherapy. 31095341 2020
dbSNP: rs12128526
rs12128526
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1891215
rs1891215
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C1305855
Disease:
Body mass index
T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs7534398
rs7534398
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
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: rs12137398
rs12137398
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C1269683
Disease:
Major Depressive Disorder
T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs12137398
rs12137398
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0525045
Disease:
Mood Disorders
T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs4908678
rs4908678
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0428883
Disease:
Diastolic blood pressure
T 0.700 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653 2018
dbSNP: rs6691442
rs6691442
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
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: rs7512599
rs7512599
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C1269683
Disease:
Major Depressive Disorder
A 0.700 GeneticVariation GWASCAT Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways. 29662059 2018
dbSNP: rs185305928
rs185305928
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C4277682
Disease:
Chemical and Drug Induced Liver Injury
0.700 GeneticVariation GWASCAT Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study. 28043905 2017
dbSNP: rs10864302
rs10864302
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C1863416
Disease:
Autosomal dominant compelling helio ophthalmic outburst syndrome
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs11121012
rs11121012
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C3828530
Disease:
Platelet Component Distribution Width Measurement
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11121012
rs11121012
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0200665
Disease:
Platelet mean volume determination (procedure)
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2412208
rs2412208
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C1862939
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 1
0.700 GeneticVariation GWASCAT Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis. 27244217 2016
dbSNP: rs2412208
rs2412208
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C3542025
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
0.700 GeneticVariation GWASCAT Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis. 27244217 2016
dbSNP: rs2412208
rs2412208
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.700 GeneticVariation GWASCAT Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis. 27244217 2016
dbSNP: rs2412208
rs2412208
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C1862941
Disease:
Amyotrophic Lateral Sclerosis, Sporadic
0.700 GeneticVariation GWASCAT Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis. 27244217 2016
dbSNP: rs1135401818
rs1135401818
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C3553661
Disease:
CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION
T 0.700 GeneticVariation CLINVAR Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes. 24738973 2015
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes. 24738973 2015
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes. 24738973 2015
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR Neuropsychological and neuroimaging phenotype induced by a CAMTA1 mutation. 24145135 2014
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR Ataxia and Purkinje cell degeneration in mice lacking the CAMTA1 transcription factor. 25049392 2014
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR Ataxia and Purkinje cell degeneration in mice lacking the CAMTA1 transcription factor. 25049392 2014
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR Neuropsychological and neuroimaging phenotype induced by a CAMTA1 mutation. 24145135 2014
dbSNP: rs11120822
rs11120822
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C1281901
Disease:
Fatty acid measurement
C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium. 23362303 2013