Annotation Detail

Information
Associated Genes
Associated Variants
NM_000130.4(F5):c.1601G>A (p.Arg534Gln) AND Ischemic stroke
NM_000130.5(F5):c.1601= (p.Arg534=) AND not provided
Source Database
GWAS Catalog
Description
A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.
GWAS Strongest risk allele
rs6025-T
GWAS Catalog disease or trait
Venous thromboembolism
GWAS Catalog p-Value
2E-22
GWAS Odds ratio OR beta coefficient
3.57
GWAS 95% confidence interval
[2.76-4.60]
GWAS parent term
Cardiovascular disease
URL
http://www.ebi.ac.uk/efo/EFO_0004286
Drugs