BRD1, bromodomain containing 1, 23774

N. diseases: 50; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs138880
rs138880
Entrez Id: 23774
Gene Symbol: BRD1
BRD1
CUI: C0036341
Disease:
Schizophrenia 		0.820 GeneticVariation BEFREE DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele. 28095495 2017
dbSNP: rs138880
rs138880
Entrez Id: 23774
Gene Symbol: BRD1
BRD1
CUI: C0036341
Disease:
Schizophrenia 		C 0.820 GeneticVariation GWASDB A comprehensive family-based replication study of schizophrenia genes. 23894747 2013
dbSNP: rs138880
rs138880
Entrez Id: 23774
Gene Symbol: BRD1
BRD1
CUI: C0036341
Disease:
Schizophrenia 		C 0.820 GeneticVariation GWASCAT A comprehensive family-based replication study of schizophrenia genes. 23894747 2013
dbSNP: rs138880
rs138880
Entrez Id: 23774
Gene Symbol: BRD1
BRD1
CUI: C0036341
Disease:
Schizophrenia 		0.820 GeneticVariation BEFREE Although the SNP (rs138880) that previously has been associated with schizophrenia showed the same trend in the Japanese population, no significant association was detected between BRD1 and schizophrenia in our study. 19908236 2010
dbSNP: rs138834
rs138834
Entrez Id: 23774
Gene Symbol: BRD1
BRD1
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4468
rs4468
Entrez Id: 23774
Gene Symbol: BRD1
BRD1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs138857
rs138857
Entrez Id: 23774
Gene Symbol: BRD1
BRD1
CUI: C0200665
Disease:
Platelet mean volume determination (procedure) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs4468
rs4468
Entrez Id: 23774
Gene Symbol: BRD1
BRD1
CUI: C1269683
Disease:
Major Depressive Disorder 		0.010 GeneticVariation BEFREE We measured COMT gene methylation and polymorphisms (Val158Met) at the rs4468 locus in peripheral blood samples of healthy controls (n = 90) and patients with MDD (n = 90). 29723539 2018