rs112193369
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Prostate carcinoma
0.700
GeneticVariation
GWASCAT
Radiogenomics Consortium Genome-Wide Association Study Meta-Analysis of Late Toxicity After Prostate Cancer Radiotherapy.
31095341
2020
rs12128526
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Body mass index
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs1891215
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
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
rs7534398
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
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
rs12137398
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
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
rs12137398
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
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
rs4908678
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
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
rs6691442
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
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
rs7512599
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
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
rs185305928
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
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
rs10864302
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Autosomal dominant compelling helio ophthalmic outburst syndrome
0.700
GeneticVariation
GWASCAT
Detection and interpretation of shared genetic influences on 42 human traits.
27182965
2016
rs11121012
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
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
rs11121012
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
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
rs2412208
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
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
rs2412208
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
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
rs2412208
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
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
rs2412208
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
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
rs2412208
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Amyotrophic Lateral Sclerosis
0.010
GeneticVariation
BEFREE
Among the 4256 patients included in the analysis (2589 male [60.8%] and 1667 female [39.2%]; mean [SD] age at onset, 59 [12] years), the following 2 novel loci were significantly associated with ALS survival: at 10q23 (rs139550538; P = 1.87 × 10-9) and in the CAMTA1 gene at 1p36 (rs2412208 , P = 3.53 × 10-8).
27244217
2016
rs1135401818
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION
T
0.700
GeneticVariation
CLINVAR
Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes.
24738973
2015
rs1553238271
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Dysmorphic features
T
0.700
GeneticVariation
CLINVAR
Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes.
24738973
2015
rs1553238271
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Muscle hypotonia
T
0.700
GeneticVariation
CLINVAR
Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes.
24738973
2015
rs1553238271
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Dysmorphic features
T
0.700
GeneticVariation
CLINVAR
Neuropsychological and neuroimaging phenotype induced by a CAMTA1 mutation.
24145135
2014
rs1553238271
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Dysmorphic features
T
0.700
GeneticVariation
CLINVAR
Ataxia and Purkinje cell degeneration in mice lacking the CAMTA1 transcription factor.
25049392
2014
rs1553238271
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Muscle hypotonia
T
0.700
GeneticVariation
CLINVAR
Ataxia and Purkinje cell degeneration in mice lacking the CAMTA1 transcription factor.
25049392
2014
rs1553238271
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Muscle hypotonia
T
0.700
GeneticVariation
CLINVAR
Neuropsychological and neuroimaging phenotype induced by a CAMTA1 mutation.
24145135
2014