rs757240974, F2

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Factor II deficiency
CUI: C3203356
Disease: Factor II deficiency
4 0.851 0.080 11 46728060 missense variant C/T snv 4.1E-06 0.010 1.000 1 1996 1996
Factor X Deficiency
CUI: C0015519
Disease: Factor X Deficiency
27 0.851 0.080 11 46728060 missense variant C/T snv 4.1E-06 0.010 1.000 1 2006 2006
Hypoprothrombinemias
CUI: C4722227
Disease: Hypoprothrombinemias
5 0.851 0.080 11 46728060 missense variant C/T snv 4.1E-06 0.010 1.000 1 1996 1996
Inherited Factor II deficiency
CUI: C0020640
Disease: Inherited Factor II deficiency
13 0.851 0.080 11 46728060 missense variant C/T snv 4.1E-06 0.010 1.000 1 1996 1996