present in Gene: FUNDC2
present in Chromosome: X
Position on Chromosome: 155050522
Alleles of this Variant: T/C
rs114209171 in
FUNDC2 gene and
Cerebrovascular accident
PMID 26908601 2016 Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
rs114209171 in
FUNDC2 gene and
Deep Vein Thrombosis
PMID 26908601 2016 Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
rs114209171 in
FUNDC2 gene and
Ischemic stroke
PMID 26908601 2016 Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
rs114209171 in
FUNDC2 gene and
Pulmonary Embolism
PMID 26908601 2016 Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
rs114209171 in
FUNDC2 gene and
Venous Thromboembolism
PMID 26908601 2016 Among the genome-wide significant results, our study replicated previously known venous thromboembolism (VTE) loci near the F5, FGA-FGG, F11, F2, PROCR and ABO genes, and the more recently discovered locus near SLC44A2 In addition, our study reports for the first time a genome-wide significant association between rs114209171, located upstream of the F8 structural gene, and thrombosis risk.