FGG, fibrinogen gamma chain, 2266

N. diseases: 70; N. variants: 18
Source: ALL
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: rs2066865
rs2066865
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
Cardiovascular Diseases 0.860 0.900 10 2011 2019
dbSNP: rs2066864
rs2066864
4 154604543 3 prime UTR variant G/A snv 0.26
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
Cardiovascular Diseases 0.800 1.000 2 2011 2019
dbSNP: rs2066861
rs2066861
4 154606284 intron variant C/T snv 0.26
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
Cardiovascular Diseases 0.700 1.000 1 2011 2011