Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10038113 1.000 0.040 5 25902233 intergenic variant T/C snv 0.45 1
rs10058083 1.000 0.040 5 25894289 intergenic variant G/A snv 0.38 1
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs10185592 1.000 0.040 2 205829457 intergenic variant A/C snv 0.11 1
rs10205350 1.000 0.040 2 30923631 intron variant G/T snv 0.24 1
rs10239799 1.000 0.040 7 120765281 intergenic variant C/T snv 0.37 1
rs10489525 1.000 0.040 1 114721064 intron variant G/A snv 0.32 1
rs10498676 0.925 0.040 6 11026766 intron variant G/A snv 0.18 3
rs10500171 1.000 0.040 7 147183313 intron variant A/G snv 0.52 1
rs10513025 1.000 0.040 5 9623510 non coding transcript exon variant T/C snv 5.4E-02 1
rs1051312 0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 5
rs1053972 1.000 0.040 19 50855373 3 prime UTR variant C/T snv 0.24 1
rs1057518345 0.742 0.400 20 50894172 frameshift variant ACTA/- delins 25
rs1057518658 1.000 0.040 2 165331409 frameshift variant AC/- del 1
rs1057518993 1.000 0.040 X 53243367 stop gained G/A snv 1
rs1057518999 1.000 0.040 3 70977826 splice donor variant A/G snv 1
rs1057519440 1.000 0.040 X 51744647 missense variant G/A snv 3
rs1057521223 1.000 0.040 2 165373339 stop gained G/A;T snv 5
rs1060499733 0.851 0.120 3 47846757 missense variant A/G snv 11
rs1060826 0.851 0.160 17 27762841 synonymous variant T/C snv 0.66 0.67 4
rs1064793345 0.752 0.240 10 87961039 missense variant T/C snv 11
rs1064794245 1.000 0.040 22 40349918 missense variant A/C snv 1
rs1064794254 0.851 0.120 X 119841185 frameshift variant CT/- delins 6
rs10732392 1.000 0.040 9 126633758 intron variant A/G snv 0.84 1
rs10749886 1.000 0.040 11 107129809 intergenic variant G/A snv 0.35 1