Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10496632
rs10496632
Entrez Id: 129684
Gene Symbol: CNTNAP5
CNTNAP5
CUI: C0596887
Disease:
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
dbSNP: rs10496632
rs10496632
Entrez Id: 129684
Gene Symbol: CNTNAP5
CNTNAP5
CUI: C0596887
Disease:
mathematical ability 		C 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: rs11123030
rs11123030
Entrez Id: 129684
Gene Symbol: CNTNAP5
CNTNAP5
CUI: C1269683
Disease:
Major Depressive Disorder 		C 0.700 GeneticVariation GWASCAT Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways. 29662059 2018
dbSNP: rs12711680
rs12711680
Entrez Id: 129684
Gene Symbol: CNTNAP5
CNTNAP5
CUI: C0036341
Disease:
Schizophrenia 		G 0.700 GeneticVariation GWASCAT Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study. 29503163 2018
dbSNP: rs4848924
rs4848924
Entrez Id: 129684
Gene Symbol: CNTNAP5
CNTNAP5
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: rs11899245
rs11899245
Entrez Id: 129684
Gene Symbol: CNTNAP5
CNTNAP5
CUI: C0201968
Disease:
Cortisol Measurement 		T 0.700 GeneticVariation GWASCAT The low single nucleotide polymorphism heritability of plasma and saliva cortisol levels. 28843169 2017
dbSNP: rs10178249
rs10178249
Entrez Id: 129684
Gene Symbol: CNTNAP5
CNTNAP5
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASDB Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). 21738479 2011
dbSNP: rs13002390
rs13002390
Entrez Id: 129684
Gene Symbol: CNTNAP5
CNTNAP5
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASDB Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). 21738479 2011
dbSNP: rs13407611
rs13407611
Entrez Id: 129684
Gene Symbol: CNTNAP5
CNTNAP5
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASDB Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). 21738479 2011
dbSNP: rs1993273
rs1993273
Entrez Id: 129684
Gene Symbol: CNTNAP5
CNTNAP5
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASDB Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). 21738479 2011
dbSNP: rs2420864
rs2420864
Entrez Id: 129684
Gene Symbol: CNTNAP5
CNTNAP5
CUI: C0025303
Disease:
Meningococcal Infections 		0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010