Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs905880501 0.827 0.200 1 119422501 stop gained C/T snv 5
rs756607591 0.882 0.200 1 119415454 missense variant G/A snv 4.0E-06 2.2E-04 3
rs757033996 0.882 0.200 1 119419519 missense variant G/A snv 2.0E-05 4.9E-05 3
rs1351141519 0.882 0.200 2 25161718 missense variant G/C snv 3
rs1465262924 0.925 0.240 1 6281155 missense variant T/G snv 2
rs201988564 0.925 0.240 5 128464739 missense variant T/G snv 1.2E-05 2.1E-05 2
rs765547422 0.925 0.200 1 119422166 missense variant C/A snv 1.2E-05 2
rs121964896 1.000 0.200 1 119422243 missense variant GT/AA mnv 1
rs121964897 1.000 0.200 1 119422523 missense variant C/T snv 1
rs1388517943 1.000 0.200 1 119419574 missense variant A/G snv 8.0E-06 7.0E-06 1
rs1399005702 1.000 0.200 1 119422258 missense variant T/A snv 1.2E-05 1
rs1411029929 1.000 0.200 1 119422261 missense variant T/A;G snv 4.0E-06; 4.0E-06 1
rs28934880 1.000 0.200 1 119415448 missense variant C/A;T snv 1.2E-05; 4.0E-06 1
rs35486059 1.000 0.200 1 119422001 missense variant C/A;T snv 4.0E-06; 1.4E-03 1
rs35887327 1.000 0.200 1 119422208 missense variant T/C snv 3.0E-03 1.3E-02 1
rs587628683 1.000 0.200 1 119421886 missense variant G/A snv 3.6E-05 1.4E-05 1
rs759422374 1.000 0.200 1 119422138 missense variant A/G snv 2.0E-05 7.0E-06 1
rs762479018 1.000 0.200 1 119422019 missense variant T/G snv 2.8E-05 4.2E-05 1
rs767128094 1.000 0.200 1 119422565 stop gained G/A snv 8.0E-06 1
rs779418168 1.000 0.200 1 119421965 missense variant C/T snv 4.0E-06 1
rs80358216 1.000 0.200 1 119422013 stop gained G/A snv 1
rs80358218 1.000 0.200 1 119422620 stop lost A/C;G snv 4.0E-06; 4.0E-06 1
rs80358219 1.000 0.200 1 119421925 stop gained G/A;T snv 1.2E-05; 4.0E-06 1
rs80358220 1.000 0.200 1 119422165 missense variant C/A;G snv 4.0E-06 1
rs80358221 1.000 0.200 1 119422277 missense variant C/T snv 1.2E-05 1.4E-05 1