Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11646213 0.827 0.320 16 82609046 intergenic variant A/T snv 0.47 6
rs1454694 0.827 0.080 4 181276794 intergenic variant T/C snv 0.20 5
rs9295740 0.827 0.120 6 27721723 intergenic variant G/A snv 0.27 5
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 3
rs10429489 0.925 0.080 9 21787522 intergenic variant G/A snv 0.26 2
rs10503380 1.000 0.080 8 9552985 upstream gene variant C/T snv 0.25 2
rs11991621 1.000 0.080 8 9549072 intergenic variant C/T snv 0.18 2
rs12621220 1.000 0.080 2 112840678 non coding transcript exon variant C/T snv 0.24 2
rs17635492 1.000 0.080 6 117450114 intron variant A/T snv 2.4E-02 2
rs2018683 1.000 0.080 7 28974579 intergenic variant G/A;T snv 2
rs2270628 0.925 0.120 7 45909971 downstream gene variant C/T snv 0.25 2
rs344924 1.000 0.080 1 67639770 intergenic variant A/G snv 0.17 2
rs6601328 1.000 0.080 8 9545693 regulatory region variant G/A;C snv 2
rs7040869 1.000 0.080 9 99072866 downstream gene variant G/A snv 0.11 2
rs7186128 1.000 0.080 16 16864058 intergenic variant G/A snv 0.70 2
rs10878232 1.000 0.080 12 65128867 intergenic variant T/A;C;G snv 1
rs11674251 1.000 0.080 2 20016748 upstream gene variant T/C snv 0.18 1
rs12000445 1.000 0.080 9 23426273 intron variant A/G snv 0.18 1
rs1209950 1.000 0.080 21 38801604 upstream gene variant C/T snv 0.30 1
rs1414493 1.000 0.080 1 241523216 upstream gene variant A/G snv 0.62 1
rs1957860 1.000 0.080 14 53962637 upstream gene variant C/T snv 0.51 1
rs4743325 1.000 0.080 9 99087445 intergenic variant G/T snv 0.24 1
rs6122390 1.000 0.080 20 63173912 intron variant C/T snv 0.27 1
rs7629386 1.000 0.080 3 40925416 regulatory region variant C/T snv 0.30 1
rs9660710 1.000 0.080 1 1163962 upstream gene variant A/C;T snv 1