Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10423928 0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs1800779 0.763 0.320 7 150992855 intron variant G/A;C snv 9
rs140226130 0.790 0.200 18 33336845 intron variant -/CTTTTTGCT delins 7.8E-02 8
rs16867253 0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 7
rs12564445 0.851 0.040 1 201376359 intron variant G/A snv 0.27 5
rs1860561 0.851 0.080 12 110345436 intron variant G/A snv 0.19 5
rs2149954 0.882 0.080 5 158393594 intron variant C/T snv 0.37 5
rs740363 0.851 0.080 10 116816095 intron variant G/A snv 0.40 5
rs1739843 0.882 0.040 1 16016759 intron variant T/C snv 0.62 4
rs9838915 0.882 0.120 3 126347377 intron variant G/A snv 0.19 4
rs10501920 0.882 0.080 11 99622442 intron variant C/G snv 0.14 3
rs11110004 1.000 0.040 12 99694540 intron variant T/C snv 5.1E-03 3
rs112434206 1.000 0.040 5 33083283 intron variant A/C;G snv 7.6E-03 3
rs113235453 1.000 0.040 14 31849939 intron variant A/G snv 3.5E-02 3
rs149322277 1.000 0.040 16 87925065 intron variant C/T snv 5.6E-03 3
rs149447933 1.000 0.040 6 14453908 intron variant C/G snv 4.4E-03 3
rs150109621 1.000 0.040 22 46429532 intron variant C/T snv 5.9E-03 3
rs150381023 1.000 0.040 22 46423108 intron variant T/C snv 5.8E-03 3
rs16917667 1.000 0.040 8 95439600 intron variant G/A snv 4.1E-02 3
rs1700575 1.000 0.040 5 8543925 intron variant A/T snv 0.26 3
rs535263906 1.000 0.040 22 46422493 intron variant G/A snv 8.6E-03 3
rs6026584 0.925 0.040 20 58894018 intron variant T/C snv 0.70 3
rs61823501 1.000 0.040 1 184396836 intron variant C/T snv 0.12 3
rs74864598 1.000 0.040 8 95439207 intron variant C/A snv 4.4E-02 3
rs7965830 1.000 0.040 12 75962050 intron variant C/A;T snv 3