Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886424 0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 10
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs10275045 0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs2524005 0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 5
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 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
rs4356203 0.925 0.040 11 17138601 intron variant A/G snv 0.31 4
rs6484218 0.882 0.040 11 10369034 intron variant G/A snv 0.21 4
rs7219021 0.925 0.040 17 48763179 intron variant T/G snv 0.26 4
rs7872515 0.925 0.040 9 92060258 intron variant G/A snv 0.25 4