Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763820362 1.000 0.040 1 151424045 missense variant C/T snv 2.4E-05 1
rs760059077 1.000 0.040 1 151405919 missense variant C/T snv 2.4E-05 2.1E-05 1
rs866632178 1.000 0.040 1 151441000 missense variant C/T snv 1.6E-05 1.4E-05 1
rs574335012 1.000 0.040 1 151427959 missense variant G/C snv 1.2E-05 1
rs888864913 1.000 0.040 1 151424097 missense variant C/T snv 1.2E-05 2.8E-05 1
rs548226228 1.000 0.040 1 151406914 missense variant G/A snv 1.2E-05 2.1E-05 1
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs202098093 1.000 0.040 1 151405476 missense variant G/A snv 1.2E-05 7.0E-06 1
rs760211123 1.000 0.040 1 151405662 missense variant T/C snv 1.2E-05 7.0E-06 1
rs753214391 1.000 0.040 1 151406444 missense variant C/T snv 1.0E-05 2.1E-05 1
rs998675361 1.000 0.040 1 151430806 missense variant G/A;C snv 9.0E-06 1
rs754532606 1.000 0.040 1 151423526 missense variant C/T snv 8.0E-06 2.1E-05 1
rs756691187 1.000 0.040 1 151404993 missense variant C/G snv 8.0E-06 7.0E-06 1
rs28934908 0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 12
rs1452048149 1.000 0.040 1 151404828 missense variant C/T snv 4.0E-06 1
rs749548928 1.000 0.040 1 151408815 missense variant T/C;G snv 4.0E-06 1
rs1396313317 1.000 0.040 7 147562137 splice acceptor variant G/A;C snv 4.0E-06 1
rs375045125 1.000 0.040 1 151429672 missense variant T/C snv 4.0E-06 7.0E-06 1
rs370498156 1.000 0.040 1 151404903 missense variant T/C;G snv 4.0E-06 1.4E-05 1
rs769236847 0.807 0.200 7 97869011 missense variant C/T snv 4.0E-06 3.5E-05 1
rs121912562 0.925 0.160 4 148435252 stop gained G/A;C snv 4.0E-06 2
rs121909231 0.667 0.600 10 87961095 stop gained C/A;T snv 29
rs121909219 0.689 0.400 10 87957915 stop gained C/A;T snv 24
rs1085308043 0.763 0.200 10 87925511 splice acceptor variant A/G;T snv 12
rs112795301 0.776 0.160 3 70972634 stop gained G/A snv 11