Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519941 0.776 0.240 3 179203761 missense variant T/C;G snv 10
rs1057519995 0.807 0.240 17 7674200 missense variant T/A snv 9
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs985033810 0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057519997 0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 24
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs730882025 0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121912655 0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 12
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs587780073 0.708 0.400 17 7674262 missense variant T/C;G snv 19
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs193920774 0.695 0.440 17 7673823 missense variant C/A;T snv 22
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31