Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs387906675
rs387906675
PROS1
3 0.882 0.080 3 93900830 missense variant T/C snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs72547528
rs72547528
VKORC1 ; PRSS53
3 0.925 0.120 16 31091334 missense variant G/A;C snv 7.2E-05; 8.1E-06 0.010 1.000 1 2015 2015