F2, coagulation factor II, thrombin, 2147

N. diseases: 61; N. variants: 24
Disease: Venous Thromboembolism ×
Source: CURATED ×
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1799963
rs1799963 		0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.730 1.000 5 2012 2019
dbSNP: rs3136516
rs3136516 		1.000 0.080 11 46739206 intron variant G/A snv 0.38
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 2 2017 2019