Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10683701
OS9
1.000 0.120 12 57698305 intron variant -/ACTT delins 0.61 1
rs5844572 0.752 0.360 22 23893562 intron variant -/ATTC delins 11
rs574503121 1.000 0.120 6 33090337 downstream gene variant -/ATTT delins 4.3E-04 1
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs373094430 1.000 0.120 6 32622847 TF binding site variant -/C ins 1
rs201386475 1.000 0.120 6 32668286 5 prime UTR variant -/CA delins 1
rs112630268 1.000 0.120 13 113919624 non coding transcript exon variant -/G ins 1
rs11439060 1.000 0.120 4 87975555 non coding transcript exon variant -/G delins 1
rs397897657 1.000 0.120 21 44230126 intron variant -/G delins 1.7E-04 1
rs56323213 1.000 0.120 21 44230126 intron variant -/G delins 1
rs113652681 1.000 0.120 6 33339623 downstream gene variant -/G;TG ins 1
rs3134069 0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs1341239 0.776 0.360 6 22303975 intron variant A/C snv 0.65 8
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 7
rs6568431 0.790 0.320 6 106140931 intron variant A/C snv 0.61 7
rs3129878 0.807 0.360 6 32440958 intron variant A/C snv 0.30 6
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 6
rs2844479 0.925 0.200 6 31605179 intergenic variant A/C snv 0.34 5
rs3129871 0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs6659932 0.827 0.240 1 67336688 intron variant A/C snv 0.81 5
rs9268644 0.827 0.360 6 32440267 intron variant A/C snv 0.68 5
rs11137037 0.851 0.200 8 6538661 intron variant A/C snv 0.40 4
rs371045754
F9
0.882 0.200 X 139530726 upstream gene variant A/C snv 5.5E-06 1.9E-05 4
rs9269081 0.851 0.280 6 32473323 intron variant A/C snv 0.69 4
rs2647046 0.882 0.200 6 32700559 TF binding site variant A/C snv 0.64 3