Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs505922
rs505922
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.800 GeneticVariation GWASDB A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. 22672568

2012
dbSNP: rs505922
rs505922
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		C 0.800 GeneticVariation GWASDB Genetics of venous thrombosis: insights from a new genome wide association study. 21980494

2011
dbSNP: rs505922
rs505922
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		C 0.800 GeneticVariation GWASCAT Genetics of venous thrombosis: insights from a new genome wide association study. 21980494

2011
dbSNP: rs505922
rs505922
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		C 0.800 GeneticVariation GWASCAT Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. 19278955

2009
dbSNP: rs505922
rs505922
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		C 0.800 GeneticVariation GWASDB Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. 19278955

2009