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: rs121918453
rs121918453
0.732 0.280 12 112450394 missense variant G/A;C;T snv
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation
0.700 0
dbSNP: rs121918462
rs121918462
0.742 0.320 12 112450398 missense variant C/T snv
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation
0.700 0
dbSNP: rs397507545
rs397507545
0.708 0.560 12 112489083 missense variant G/A;C snv 4.0E-06
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation
0.700 0