Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519915 0.851 0.160 1 11109318 missense variant A/C snv 5
rs1057519914 0.851 0.240 1 11157174 missense variant A/G snv 4
rs1057519916 0.882 0.160 1 11109320 missense variant T/A snv 4
rs786205165 0.882 0.120 1 11157173 missense variant C/A;T snv 4
rs1057519913 0.925 0.120 1 11157172 missense variant G/C snv 3
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 18
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 16
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 5
rs1057520010 0.882 0.200 2 61492336 missense variant T/A;G snv 5
rs754688962 0.851 0.200 2 197402637 missense variant T/C;G snv 5
rs113994087
ALK
0.827 0.120 2 29209798 missense variant C/A;T snv 4
rs63750624 0.925 0.160 2 47410211 missense variant G/A snv 4
rs1553622530 2 214781220 stop gained C/T snv 1
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 23
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 21
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 20
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 15
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 14