Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs4072037 0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 16
rs689465 0.851 0.200 1 186681714 upstream gene variant T/C snv 0.14 7
rs1454328441 0.827 0.200 1 155192002 missense variant G/A;T snv 4.6E-06; 9.1E-06 6
rs2564978 0.827 0.080 1 207321071 upstream gene variant T/C snv 0.77 6
rs2070803 0.925 0.080 1 155185239 intron variant G/A snv 0.55 5
rs4844880 0.882 0.240 1 209697571 intron variant A/T snv 0.70 4
rs765660823 0.882 0.200 1 162778720 missense variant A/C snv 1.9E-04 4
rs586339 1.000 0.080 1 43671586 missense variant C/A;G;T snv 0.70 0.78 2
rs199647144 1 156842109 missense variant T/C;G snv 8.8E-05; 4.0E-06 1
rs3811047 0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs3087386 0.790 0.160 2 99439044 missense variant A/G snv 0.58 0.61 8
rs1057519696
ALK
1.000 0.040 2 29214054 missense variant C/T snv 5
rs759435862 0.925 0.080 2 8776852 missense variant C/A;T snv 2.0E-05 5
rs1347093 0.882 0.080 2 56019205 intron variant G/T snv 0.21 4
rs3087399 0.882 0.120 2 99438696 missense variant T/C snv 0.13 0.17 4
rs1227480017 2 10122697 synonymous variant C/A snv 1
rs12613347 2 201190589 intron variant C/T snv 0.19 1
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29