CNTN2, contactin 2, 6900

N. diseases: 99; N. variants: 14
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11240341
rs11240341
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
CUI: C0036341
Disease:
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
dbSNP: rs3903399
rs3903399
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
CUI: C0205682
Disease:
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
dbSNP: rs1572995
rs1572995
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs2071533
rs2071533
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
CUI: C2985280
Disease:
Blood Protein Measurement 		G 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs3767297
rs3767297
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
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: rs3820337
rs3820337
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
CUI: C0596887
Disease:
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
dbSNP: rs6593920
rs6593920
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
CUI: C0596887
Disease:
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
dbSNP: rs9787409
rs9787409
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs6696846
rs6696846
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
CUI: C0014772
Disease:
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
dbSNP: rs16937
rs16937
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
CUI: C0036341
Disease:
Schizophrenia 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764 2015
dbSNP: rs1042831
rs1042831
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs6662930
rs6662930
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs6696846
rs6696846
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs398122387
rs398122387
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
CUI: C3809374
Disease:
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5 		T 0.700 CausalMutation CLINVAR
dbSNP: rs2275697
rs2275697
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2
CUI: C0393819
Disease:
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