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: rs121918154
rs121918154
1.000 0.080 2 127428374 missense variant C/A;T snv 4.0E-06; 2.0E-05
CUI: C0040038
Disease: Thromboembolism
Thromboembolism
Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1553424043
rs1553424043
0.925 0.120 2 127423123 missense variant T/C snv
CUI: C0040038
Disease: Thromboembolism
Thromboembolism
Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs369504169
rs369504169
0.925 0.120 2 127421337 missense variant G/A snv 8.0E-06 7.0E-06
CUI: C0040038
Disease: Thromboembolism
Thromboembolism
Cardiovascular Diseases 0.700 1.000 1 2019 2019