Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10008257 0.925 0.040 4 94435177 intergenic variant G/A snv 0.63 2
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs13072940 0.851 0.040 3 36801132 regulatory region variant T/A snv 0.37 5
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 5
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs17066873 0.851 0.040 13 76889874 non coding transcript exon variant T/C snv 5.4E-02 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs2769605 0.827 0.040 9 85297756 intergenic variant C/T snv 0.44 5
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs6937506 0.807 0.280 6 132578260 intergenic variant G/A snv 0.25 7
rs7713917 0.925 0.040 5 79533426 upstream gene variant A/G snv 0.54 3
rs77826363 0.882 0.040 6 1128802 intergenic variant G/T snv 2.2E-02 3
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 7
rs9364726 0.882 0.040 6 164236705 intergenic variant A/G snv 6.5E-02 3
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs16875288 0.851 0.040 5 5297087 intron variant A/T snv 0.22 4
rs10994336 0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs10994338 0.882 0.040 10 60421370 intron variant G/A snv 7.5E-02 3
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs10994397 0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 5