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: rs1176447366
rs1176447366
3 0.882 0.080 1 31586845 missense variant G/A snv 0.010 1.000 1 2005 2005
dbSNP: rs757240974
rs757240974
F2
4 0.851 0.080 11 46728060 missense variant C/T snv 4.1E-06 0.010 1.000 1 1996 1996
dbSNP: rs770671957
rs770671957
F10
3 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
dbSNP: rs781413602
rs781413602
F10
3 0.882 0.080 13 113149087 missense variant G/A;T snv 1.6E-05; 4.0E-06 0.010 1.000 1 1996 1996