rs770671957, F10

N. diseases: 3
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 0.882 0.080 13 113149326 missense variant C/G;T snv 8.0E-06; 4.0E-06 0.010 1.000 1 1996 1996
Hypoprothrombinemias
CUI: C4722227
Disease: Hypoprothrombinemias
5 0.882 0.080 13 113149326 missense variant C/G;T snv 8.0E-06; 4.0E-06 0.010 1.000 1 1996 1996
Inherited Factor II deficiency
CUI: C0020640
Disease: Inherited Factor II deficiency
13 0.882 0.080 13 113149326 missense variant C/G;T snv 8.0E-06; 4.0E-06 0.010 1.000 1 1996 1996