Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893875 0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs201106962 0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 5
rs431905511 0.827 0.080 4 89828154 missense variant C/T snv 9
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs542171324 0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 6
rs2298728 1.000 0.040 4 89821664 intron variant G/A;T snv 1
rs894278 0.882 0.080 4 89813384 intron variant T/G snv 0.15 4
rs2197120 1.000 0.040 4 89808451 intron variant A/G snv 0.78 1
rs3775444 1.000 0.040 4 89805385 intron variant C/T snv 6.7E-02 1
rs3775442 1.000 0.040 4 89794080 intron variant C/T snv 6.7E-02 1
rs10014396 1.000 0.040 4 89791478 intron variant T/C snv 0.17 1
rs2737029 1.000 0.040 4 89790619 intron variant T/C snv 0.45 1
rs3775439 1.000 0.040 4 89788590 intron variant G/A snv 0.25 1
rs356186 1.000 0.040 4 89784213 intron variant A/G snv 0.80 1
rs356188 1.000 0.040 4 89770386 intron variant T/C snv 0.21 1
rs3796661 1.000 0.040 4 89766356 intron variant C/T snv 8.7E-02 1
rs10516845 1.000 0.040 4 89763127 intron variant A/G;T snv 1
rs2736990 0.882 0.080 4 89757390 intron variant G/A;T snv 4
rs3857059 1.000 0.040 4 89754087 intron variant A/G;T snv 2
rs356168 1.000 0.040 4 89753280 intron variant G/A snv 0.45 1
rs356200 0.882 0.160 4 89747463 intron variant T/C snv 0.44 4
rs356203 1.000 0.040 4 89744890 intron variant C/T snv 0.54 1
rs3822086 1.000 0.040 4 89743643 intron variant C/T snv 0.24 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