rs802568
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Mental disorders
0.800
GeneticVariation
GWASCAT
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
20889312
2010
rs802568
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Psychotic Disorders
C
0.800
GeneticVariation
GWASDB
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
20889312
2010
rs802568
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Psychotic Disorders
0.800
GeneticVariation
GWASCAT
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
20889312
2010
rs802568
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Mental disorders
C
0.800
GeneticVariation
GWASDB
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
20889312
2010
rs114360492
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Alzheimer's Disease
T
0.700
GeneticVariation
GWASCAT
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk.
30617256
2019
rs117834366
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Dementia, Vascular
A
0.700
GeneticVariation
GWASCAT
Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project.
31473137
2019
rs117834366
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Alzheimer's Disease
A
0.700
GeneticVariation
GWASCAT
Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project.
31473137
2019
rs1396313317
CNTNAP2;LOC107986721
Autism Spectrum Disorders
C
0.700
GeneticVariation
CLINVAR
Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations.
30763456
2019
rs190748049
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Low density lipoprotein cholesterol measurement
T
0.700
GeneticVariation
GWASCAT
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.
30670697
2019
rs6944674
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Body mass index
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs73453125
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Low density lipoprotein cholesterol measurement
A
0.700
GeneticVariation
GWASCAT
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
30926973
2019
rs2530313
CNTNAP2;LOC105375554
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
rs2530313
CNTNAP2;LOC105375554
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
rs34088420
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
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
rs34438057
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
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
rs34930172
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
mathematical ability
G
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
rs369675346
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Epilepsy, Rolandic
T
0.700
CausalMutation
CLINVAR
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
29358611
2018
rs540694424
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Glaucoma
C
0.700
GeneticVariation
GWASCAT
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.
30104761
2018
rs758630057
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Epilepsy, Rolandic
A
0.700
CausalMutation
CLINVAR
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
29358611
2018
rs802571
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Alzheimer's Disease
T
0.700
GeneticVariation
GWASCAT
A genome-wide association study of late-onset Alzheimer's disease in a Japanese population.
26049409
2015
rs10255956
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Serum albumin measurement
0.700
GeneticVariation
GWASDB
A genome-wide assessment of variability in human serum metabolism.
23281178
2013
rs4549702
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Body mass index
G
0.700
GeneticVariation
GWASCAT
Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.
23192594
2013
rs4549702
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Physical Activity Measurement
G
0.700
GeneticVariation
GWASCAT
Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.
23192594
2013
rs1718101
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Autistic Disorder
0.700
GeneticVariation
GWASDB
Individual common variants exert weak effects on the risk for autism spectrum disorders.
22843504
2012
rs398124268
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Pitt-Hopkins-Like Syndrome 1
A
0.700
CausalMutation
CLINVAR
Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1.
21827697
2011