Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736990 0.882 0.080 4 89757390 intron variant G/A;T snv 2
rs168552 1.000 0.040 4 89721993 intron variant C/T snv 0.80 1
rs181489 1.000 0.040 4 89713869 intron variant T/A;C snv 1
rs356169 1.000 0.040 4 89711617 intron variant G/T snv 0.72 1
rs356219 0.776 0.240 4 89716450 intron variant G/A snv 0.54 1
rs356220 0.925 0.080 4 89720189 intron variant T/A;C snv 1
rs356221 1.000 0.040 4 89721313 intron variant A/T snv 0.44 1
rs10516845 1.000 0.040 4 89763127 intron variant A/G;T snv 1
rs2197120 1.000 0.040 4 89808451 intron variant A/G snv 0.78 1
rs2298728 1.000 0.040 4 89821664 intron variant G/A;T snv 1
rs2737029 1.000 0.040 4 89790619 intron variant T/C snv 0.45 1
rs356165 0.882 0.080 4 89725735 3 prime UTR variant G/A snv 0.54 1
rs356168 1.000 0.040 4 89753280 intron variant G/A snv 0.45 1
rs356188 1.000 0.040 4 89770386 intron variant T/C snv 0.21 1
rs356200 0.882 0.160 4 89747463 intron variant T/C snv 0.44 1
rs356203 1.000 0.040 4 89744890 intron variant C/T snv 0.54 1
rs356204 1.000 0.040 4 89742391 intron variant T/C snv 0.44 1
rs3775423 1.000 0.040 4 89736340 intron variant C/T snv 0.24 1
rs3775439 1.000 0.040 4 89788590 intron variant G/A snv 0.25 1
rs3796661 1.000 0.040 4 89766356 intron variant C/T snv 8.7E-02 1
rs3822086 1.000 0.040 4 89743643 intron variant C/T snv 0.24 1
rs3857053 1.000 0.040 4 89724523 3 prime UTR variant C/T snv 0.24 1
rs3857059 1.000 0.040 4 89754087 intron variant A/G;T snv 1
rs7684318 1.000 0.040 4 89733852 intron variant T/C snv 0.19 1
rs894278 0.882 0.080 4 89813384 intron variant T/G snv 0.15 1