Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11120822
rs11120822
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0202177
Disease:
Phospholipid measurement
C 0.700 GeneticVariation GWASDB 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
dbSNP: rs12563101
rs12563101
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR Intragenic CAMTA1 rearrangements cause non-progressive congenital ataxia with or without intellectual disability. 22693284 2012
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR Intragenic CAMTA1 rearrangements cause non-progressive congenital ataxia with or without intellectual disability. 22693284 2012
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders. 22031302 2011
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders. 22031302 2011
dbSNP: rs1193179
rs1193179
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation GWASDB Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans. 19184112 2009
dbSNP: rs1193179
rs1193179
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation GWASDB A genome-wide association study identifies novel risk loci for type 2 diabetes. 17293876 2007
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance. 17470457 2007
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR A potential dimerization region of dCAMTA is critical for termination of fly visual response. 17537720 2007
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR A potential dimerization region of dCAMTA is critical for termination of fly visual response. 17537720 2007
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance. 17470457 2007
dbSNP: rs7547519
rs7547519
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0561843
Disease:
Memory, Episodic
0.700 GeneticVariation GWASDB Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance. 17470457 2007
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR The transcriptional coactivator CAMTA2 stimulates cardiac growth by opposing class II histone deacetylases. 16678093 2006
dbSNP: rs1553238271
rs1553238271
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 GeneticVariation CLINVAR The transcriptional coactivator CAMTA2 stimulates cardiac growth by opposing class II histone deacetylases. 16678093 2006
dbSNP: rs1553238311
rs1553238311
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C3553661
Disease:
CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION
A 0.700 GeneticVariation CLINVAR
dbSNP: rs863224853
rs863224853
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C3553661
Disease:
CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION
G 0.700 GeneticVariation CLINVAR
dbSNP: rs2412208
rs2412208
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0002736
Disease:
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
dbSNP: rs10864294
rs10864294
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE Exploration of the identified genes for the presence of disease associated variants, using Affymetrix 500K genotyping and Illumina custom genotyping arrays, highlighted a region upstream of VAMP3 within CAMTA1 to be associated with increased risk of CAD [rs10864294 P = 0.015, odds ratio (OR) = 1.30, 95% confidence interval (CI) = 1.1-1.6, 1471 cases, 2737 controls] and aggressive PD (AgP; P = 0.008, OR = 1.31, 95% CI = 1.1-1.6, 864 cases, 3664 controls). 23813974 2013
dbSNP: rs2301462
rs2301462
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE In silico replication in a meta-analysis of 14 genome-wide association studies of CAD of the CARDIoGRAM Consortium identified rs2301462, located on the same haplotype block, as associated with P = 0.001 upon adjustment for sex and age. 23813974 2013
dbSNP: rs137974312
rs137974312
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0027819
Disease:
Neuroblastoma
0.010 GeneticVariation BEFREE One CAMTA1 variant (T1336I) was not detected in 97 unaffected individuals, another (N1177K) resides in a conserved domain of the CAMTA1 protein and was found hemizygous in six neuroblastomas. 17222547 2007
dbSNP: rs41278952
rs41278952
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0027819
Disease:
Neuroblastoma
0.010 GeneticVariation BEFREE One CAMTA1 variant (T1336I) was not detected in 97 unaffected individuals, another (N1177K) resides in a conserved domain of the CAMTA1 protein and was found hemizygous in six neuroblastomas. 17222547 2007