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: rs1188383936
rs1188383936
F2
102 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs777692567
rs777692567
PLAT
5 0.827 0.200 8 42182845 missense variant G/A snv 4.0E-05 1.4E-05 0.010 1.000 1 2005 2005