SH3PXD2A, SH3 and PX domains 2A, 9644

N. diseases: 32; N. variants: 12
Disease: Atrial Fibrillation ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35176054
rs35176054
Entrez Id: 9644
Gene Symbol: SH3PXD2A
SH3PXD2A
CUI: C0004238
Disease:
Atrial Fibrillation 		A 0.700 GeneticVariation GWASCAT Multi-ethnic genome-wide association study for atrial fibrillation. 29892015 2018
dbSNP: rs35176054
rs35176054
Entrez Id: 9644
Gene Symbol: SH3PXD2A
SH3PXD2A
CUI: C0004238
Disease:
Atrial Fibrillation 		A 0.700 GeneticVariation GWASCAT Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development. 29290336 2018
dbSNP: rs35176054
rs35176054
Entrez Id: 9644
Gene Symbol: SH3PXD2A
SH3PXD2A
CUI: C0004238
Disease:
Atrial Fibrillation 		A 0.700 GeneticVariation GWASCAT Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. 30061737 2018
dbSNP: rs2047036
rs2047036
Entrez Id: 9644
Gene Symbol: SH3PXD2A
SH3PXD2A
CUI: C0004238
Disease:
Atrial Fibrillation 		G 0.700 GeneticVariation GWASCAT Identification of six new genetic loci associated with atrial fibrillation in the Japanese population. 28416822 2017
dbSNP: rs35176054
rs35176054
Entrez Id: 9644
Gene Symbol: SH3PXD2A
SH3PXD2A
CUI: C0004238
Disease:
Atrial Fibrillation 		A 0.700 GeneticVariation GWASCAT Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. 28416818 2017