Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs200638392 | 6 | 87128241 | intergenic variant | GAT/-;GATGAT | delins | 0.47 | 5 | ||||
rs201950044 | 1 | 161639782 | intergenic variant | G/T | snv | 5 | |||||
rs2082382 | 5 | 148820990 | upstream gene variant | G/A | snv | 0.72 | 5 | ||||
rs218265 | 4 | 54542832 | intergenic variant | T/C | snv | 0.21 | 9 | ||||
rs2338224 | 5 | 72432861 | intergenic variant | A/G | snv | 0.85 | 5 | ||||
rs2381416 | 1.000 | 0.080 | 9 | 6193455 | upstream gene variant | C/A | snv | 0.65 | 3 | ||
rs28383314 | 0.925 | 0.160 | 6 | 32619436 | regulatory region variant | T/C | snv | 0.61 | 4 | ||
rs2853961 | 6 | 31264212 | downstream gene variant | G/A | snv | 0.38 | 13 | ||||
rs2954031 | 8 | 125479491 | intron variant | G/T | snv | 0.42 | 8 | ||||
rs34149660 | 9 | 133001720 | intergenic variant | AAAAAAAAAAAAA/-;AAAAAA;AAAAAAA;AAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAA;AAAAAAAAAAAAAA;AAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAA | delins | 0.31 | 2 | ||||
rs34293785 | 1 | 65671509 | intergenic variant | T/C | snv | 4 | |||||
rs34332679 | 14 | 35412760 | regulatory region variant | -/A;AA | delins | 2 | |||||
rs34675278 | 5 | 98808491 | intergenic variant | AA/-;A;AAA;AAAA;AAAAA | delins | 2 | |||||
rs34762051 | 17 | 40007650 | downstream gene variant | AA/-;A;AAA | delins | 0.31 | 5 | ||||
rs35249183 | 1 | 12039288 | upstream gene variant | A/G | snv | 6.4E-02 | 2 | ||||
rs36058533 | 2 | 96570916 | intergenic variant | TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTT | delins | 2 | |||||
rs36229146 | 7 | 22744868 | downstream gene variant | AATATATATATATATATATATATATA/- | delins | 7.2E-02 | 2 | ||||
rs385893 | 0.925 | 0.080 | 9 | 4763176 | downstream gene variant | T/C | snv | 0.44 | 6 | ||
rs397933924 | 10 | 97314229 | upstream gene variant | -/CAGGTTCAAGCGA | ins | 5 | |||||
rs410867 | 19 | 16316300 | intron variant | A/G | snv | 0.32 | 2 | ||||
rs4328821 | 3 | 128597592 | intergenic variant | A/G | snv | 0.13 | 2 | ||||
rs4761234 | 12 | 69338325 | TF binding site variant | T/C | snv | 0.36 | 5 | ||||
rs4937323 | 11 | 128346797 | intergenic variant | C/T | snv | 0.53 | 2 | ||||
rs552557467 | 11 | 47927817 | regulatory region variant | AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA/-;AA;AAA;AAAA;AAAAA;AAAAAA;AAAAAAA;AAAAAAAA;AAAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAA;AAAAAAAAAAAAA;AAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA | delins | 0.47 | 4 | ||||
rs55646091 | 0.925 | 0.080 | 11 | 76588387 | upstream gene variant | G/A | snv | 3.0E-02 | 5 |