ZNF823, zinc finger protein 823, 55552

N. diseases: 4; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72986630
rs72986630
Entrez Id: 55552
Gene Symbol: ZNF823
ZNF823
CUI: C0021704
Disease:
Intelligence
0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs72986630
rs72986630
Entrez Id: 55552
Gene Symbol: ZNF823
ZNF823
CUI: C0036341
Disease:
Schizophrenia
0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs72986630
rs72986630
Entrez Id: 55552
Gene Symbol: ZNF823
ZNF823
CUI: C0036341
Disease:
Schizophrenia
T 0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs72986630
rs72986630
Entrez Id: 55552
Gene Symbol: ZNF823
ZNF823
CUI: C0008074
Disease:
Child Development Disorders, Pervasive
T 0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs72986630
rs72986630
Entrez Id: 55552
Gene Symbol: ZNF823
ZNF823
CUI: C0036341
Disease:
Schizophrenia
T 0.700 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764 2015
dbSNP: rs286262
rs286262
Entrez Id: 55552
Gene Symbol: ZNF823
ZNF823
CUI: C0020445
Disease:
Hypercholesterolemia, Familial
0.700 GeneticVariation GWASDB Low-density lipoprotein receptor mutations generate synthetic genome-wide associations. 22968135 2013
dbSNP: rs4804636
rs4804636
Entrez Id: 55552
Gene Symbol: ZNF823
ZNF823
CUI: C0020445
Disease:
Hypercholesterolemia, Familial
0.700 GeneticVariation GWASDB Low-density lipoprotein receptor mutations generate synthetic genome-wide associations. 22968135 2013