Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs11789399 0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 4
rs12966547 0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 7
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs2054399 0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs2239547 0.882 0.040 3 52821213 intron variant T/C snv 0.27 6
rs3788533 0.925 0.040 22 38127239 non coding transcript exon variant C/G snv 0.47 3
rs4356203 0.925 0.040 11 17138601 intron variant A/G snv 0.31 4
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs4765905 0.827 0.040 12 2240418 intron variant G/A;C snv 6
rs6465084 0.851 0.040 7 86774159 intron variant A/G snv 0.26 5
rs6484218 0.882 0.040 11 10369034 intron variant G/A snv 0.21 5
rs7219021 0.925 0.040 17 48763179 intron variant T/G snv 0.26 4
rs778294 0.851 0.040 13 105489886 synonymous variant C/A;T snv 0.27; 4.0E-06 0.26 5
rs7872515 0.925 0.040 9 92060258 intron variant G/A snv 0.25 4
rs802568 0.925 0.040 7 146262151 intron variant T/G snv 0.17 4
rs947267 0.882 0.040 13 105487313 intron variant T/G snv 0.51 4
rs1039002 0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs2391191 0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs2251219 0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 14