rs1042831
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
Corpuscular Hemoglobin Concentration Mean
0.700
GeneticVariation
GWASDB
Seventy-five genetic loci influencing the human red blood cell.
23222517
2012
rs11240341
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
Schizophrenia
T
0.700
GeneticVariation
GWASCAT
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
30285260
2019
rs1572995
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
Blood Protein Measurement
T
0.700
GeneticVariation
GWASCAT
Co-regulatory networks of human serum proteins link genetics to disease.
30072576
2018
rs16937
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
Schizophrenia
A
0.700
GeneticVariation
GWASCAT
Genome-wide association study of schizophrenia in Ashkenazi Jews.
26198764
2015
rs2071533
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
Blood Protein Measurement
G
0.700
GeneticVariation
GWASCAT
Genomic atlas of the human plasma proteome.
29875488
2018
rs2275697
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
0.010
GeneticVariation
BEFREE
The single-nucleotide polymorphism (SNP) rs2275697 in the transient axonal glycoprotein-1 (TAG-1) gene was reported to be associated with responsiveness to intravenous immunoglobulin (IVIG) treatment in patients with chronic inflammatory demyelinating polyneuropathy (CIDP ).
22462668
2012
rs3767297
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
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
rs3820337
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
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
rs3903399
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
Waist-Hip Ratio
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
rs398122387
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5
T
0.700
CausalMutation
CLINVAR
rs6593920
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
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
rs6662930
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
Corpuscular Hemoglobin Concentration Mean
0.700
GeneticVariation
GWASDB
Seventy-five genetic loci influencing the human red blood cell.
23222517
2012
rs6696846
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
Corpuscular Hemoglobin Concentration Mean
0.700
GeneticVariation
GWASDB
Seventy-five genetic loci influencing the human red blood cell.
23222517
2012
rs6696846
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
Red Blood Cell Count measurement
T
0.700
GeneticVariation
GWASCAT
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
27863252
2016
rs9787409
×
Entrez Id:
6900
Gene Symbol:
CNTN2
CNTN2
Blood Protein Measurement
T
0.700
GeneticVariation
GWASCAT
Genomic atlas of the human plasma proteome.
29875488
2018