Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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