Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79184941 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 18
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs371769427 0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 9
rs759610249 0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 12
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 5
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 14
rs772110575 0.807 0.160 3 179198938 missense variant G/A;T snv 4.0E-06 6
rs747241612 0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20