RS4524 F5

Health Risk Chr 1:169542516 snv missense variant

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What This Variant Does

"Gene variants associated with deep vein thrombosis. Updated analysis of gene variants associated wit...

Associated Conditions

Thrombophilia due to activated protein C resistance

Congenital factor V deficiency

Thrombophilia due to activated protein C resistance

Congenital factor V deficiency

GWAS Studies (4)

Trait	Risk Allele	OR / Beta	P-value	Study
Sialic acid-binding Ig-like lectin 11 levels	T	OR: 0.38	1E-168	PubMed
Neuronal pentraxin-2 levels	T	OR: 0.27	2E-76	PubMed
Venous thromboembolism	T	OR: 1.14	3E-29	PubMed
Venous thromboembolism	T	OR: 1.2	3E-11	PubMed

Population Frequencies

gnomAD ALL

27.3%

1kG AFR

83.2%

1kG ALL

26.7%

1kG AMR

60.5%

1kG EAS

75.2%

1kG EUR

74.7%

1kG SAS

34.3%

Other Variants in F5