Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs932879
rs932879
Entrez Id: 23078
Gene Symbol: VWA8
VWA8
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: rs9590614
rs9590614
Entrez Id: 23078
Gene Symbol: VWA8
VWA8
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease
0.010 GeneticVariation BEFREE Two are novel associations (top single-nucleotide polymorphism rs379123 in MYO1D and rs9590614 in VMA8) located within genes that function in cell-cell signaling and cell migration, and five are in loci previously associated with chronic obstructive pulmonary disease susceptibility (HHIP, IREB2/CHRNA3, CYP2A6/ADCK, TGFB2, and MMP12). 25006744 2014
dbSNP: rs9566845
rs9566845
Entrez Id: 23078
Gene Symbol: VWA8
VWA8
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder
0.010 GeneticVariation BEFREE Furthermore, marker rs9566845 was genotyped and found associated with migraine in an independent Norwegian sample of adult attention deficit hyperactivity disorder (ADHD) patients with and without comorbid migraine (n = 131 and n = 324, respectively), OR = 2.42 (1.18-4.97), P = 0.013. 20528957 2010
dbSNP: rs9566845
rs9566845
Entrez Id: 23078
Gene Symbol: VWA8
VWA8
CUI: C0149931
Disease:
Migraine Disorders
0.010 GeneticVariation BEFREE Furthermore, marker rs9566845 was genotyped and found associated with migraine in an independent Norwegian sample of adult attention deficit hyperactivity disorder (ADHD) patients with and without comorbid migraine (n = 131 and n = 324, respectively), OR = 2.42 (1.18-4.97), P = 0.013. 20528957 2010
dbSNP: rs9566845
rs9566845
Entrez Id: 23078
Gene Symbol: VWA8
VWA8
CUI: C0865424
Disease:
Adult attention deficit hyperactivity disorder
0.010 GeneticVariation BEFREE Furthermore, marker rs9566845 was genotyped and found associated with migraine in an independent Norwegian sample of adult attention deficit hyperactivity disorder (ADHD) patients with and without comorbid migraine (n = 131 and n = 324, respectively), OR = 2.42 (1.18-4.97), P = 0.013. 20528957 2010
dbSNP: rs9566867
rs9566867
Entrez Id: 23078
Gene Symbol: VWA8
VWA8
CUI: C0149931
Disease:
Migraine Disorders
0.010 GeneticVariation BEFREE Although the level of significance was significantly reduced when using the Fisher's exact test (as a result of the low count of cases with migraine), rs9566845 P = 1.4 × 10(-5) and rs9566867 P = 1.5 × 10(-5), this region remained the most prominent finding. 20528957 2010