BRD4, bromodomain containing 4, 23476

N. diseases: 335; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62113853
rs62113853
Entrez Id: 23476
Gene Symbol: BRD4
BRD4
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs62113853
rs62113853
Entrez Id: 23476
Gene Symbol: BRD4
BRD4
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6512023
rs6512023
Entrez Id: 23476
Gene Symbol: BRD4
BRD4
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs8104223
rs8104223
Entrez Id: 23476
Gene Symbol: BRD4
BRD4
CUI: C0871470
Disease:
Systolic Pressure 		G 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs1568383758
rs1568383758
Entrez Id: 23476
Gene Symbol: BRD4
BRD4
CUI: C0349588
Disease:
Short stature 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1290547844
rs1290547844
Entrez Id: 23476
Gene Symbol: BRD4
BRD4
CUI: C0023895
Disease:
Liver diseases 		0.010 GeneticVariation BEFREE The PNPLA3 p.I148M, TM6SF2 p.E167K and MBOAT7 p.G17E variants represent genetic determinants for progressive liver diseases. 31669075 2020
dbSNP: rs368453549
rs368453549
Entrez Id: 23476
Gene Symbol: BRD4
BRD4
CUI: C0038868
Disease:
Progressive supranuclear palsy 		0.010 GeneticVariation BEFREE We have identified DCTN1 p.K56R in patients with PSP. 27132499 2016