Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35761398 | 0.701 | 0.520 | 1 | 23875429 | missense variant | TT/CC | mnv | 19 | |||
rs879761216 | 0.732 | 0.480 | 1 | 23875429 | frameshift variant | TT/C;T | delins | 14 | |||
rs1946518 | 0.602 | 0.760 | 11 | 112164735 | intron variant | T/G | snv | 0.60 | 46 | ||
rs9275141 | 0.827 | 0.240 | 6 | 32683340 | intergenic variant | T/G | snv | 0.50 | 6 | ||
rs11712165 | 0.882 | 0.200 | 3 | 119399949 | intron variant | T/G | snv | 0.30 | 5 | ||
rs2074404 | 0.925 | 0.120 | 17 | 46788073 | intron variant | T/G | snv | 0.27 | 4 | ||
rs2249937 | 1.000 | 0.080 | 6 | 159094277 | non coding transcript exon variant | T/G | snv | 0.76 | 3 | ||
rs6726160 | 1.000 | 0.080 | 2 | 60937594 | non coding transcript exon variant | T/G | snv | 0.47 | 3 | ||
rs2501432 | 0.716 | 0.480 | 1 | 23875430 | missense variant | T/C;G | snv | 0.62 | 16 | ||
rs1332099 | 0.724 | 0.240 | 10 | 99538694 | downstream gene variant | T/C;G | snv | 14 | |||
rs7579944 | 0.882 | 0.200 | 2 | 30222160 | intergenic variant | T/C;G | snv | 5 | |||
rs9457515 | 1.000 | 0.080 | 6 | 158913093 | intron variant | T/C;G | snv | 1 | |||
rs12232497 | 0.701 | 0.360 | 17 | 39883866 | intergenic variant | T/C | snv | 0.35 | 18 | ||
rs12928404 | 0.724 | 0.240 | 16 | 28835925 | splice region variant | T/C | snv | 0.44 | 0.45 | 15 | |
rs10822050 | 0.724 | 0.240 | 10 | 62679011 | downstream gene variant | T/C | snv | 0.33 | 14 | ||
rs11839053 | 0.724 | 0.240 | 13 | 106410694 | intergenic variant | T/C | snv | 7.0E-02 | 14 | ||
rs2075184 | 0.724 | 0.240 | 2 | 102464132 | intergenic variant | T/C | snv | 0.78 | 14 | ||
rs6689858 | 0.724 | 0.240 | 1 | 197406337 | intron variant | T/C | snv | 0.39 | 14 | ||
rs7042370 | 0.724 | 0.240 | 9 | 12785074 | intron variant | T/C | snv | 0.58 | 14 | ||
rs7672495 | 0.724 | 0.240 | 4 | 4990640 | regulatory region variant | T/C | snv | 0.21 | 14 | ||
rs1208663703 | 0.763 | 0.200 | 22 | 37086414 | missense variant | T/C | snv | 5.2E-06 | 7.0E-06 | 9 | |
rs1738074 | 0.790 | 0.320 | 6 | 159044945 | 5 prime UTR variant | T/C | snv | 0.49 | 9 | ||
rs1800693 | 0.776 | 0.360 | 12 | 6330843 | non coding transcript exon variant | T/C | snv | 0.36; 4.0E-06 | 0.38 | 9 | |
rs4819388 | 0.790 | 0.240 | 21 | 44227538 | 3 prime UTR variant | T/C | snv | 9 | |||
rs6651252 | 0.790 | 0.200 | 8 | 128554935 | intron variant | T/C | snv | 0.19 | 8 |