Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs145013566 | 2 | 218297998 | intron variant | -/C | ins | 5 | |||||
rs397933924 | 10 | 97314229 | upstream gene variant | -/CAGGTTCAAGCGA | ins | 5 | |||||
rs3840870 | 17 | 50184820 | 3 prime UTR variant | -/CTTG | delins | 13 | |||||
rs71579625 | 1 | 158666062 | intron variant | -/G | delins | 1 | |||||
rs34338164 | 2 | 68388414 | missense variant | A/C | snv | 8.0E-03 | 7.8E-03 | 4 | |||
rs56232812 | 1 | 27859995 | intergenic variant | A/C | snv | 0.11 | 4 | ||||
rs4805881 | 19 | 33405526 | intron variant | A/C | snv | 0.69 | 3 | ||||
rs17041439 | 12 | 101479462 | intron variant | A/C | snv | 7.0E-02 | 2 | ||||
rs3845624 | 1 | 159248476 | regulatory region variant | A/C | snv | 0.57 | 2 | ||||
rs77940566 | 6 | 42542864 | intergenic variant | A/C | snv | 0.21 | 2 | ||||
rs1016680 | 17 | 37514283 | downstream gene variant | A/C | snv | 0.74 | 1 | ||||
rs10273974 | 7 | 139050766 | intron variant | A/C | snv | 0.48 | 1 | ||||
rs11264673 | 1 | 157309332 | intron variant | A/C | snv | 0.41 | 1 | ||||
rs113164910 | 6 | 32459228 | downstream gene variant | A/C | snv | 1 | |||||
rs12130298 | 1 | 117001709 | upstream gene variant | A/C | snv | 5.0E-02 | 1 | ||||
rs1410869 | 1 | 153197120 | intergenic variant | A/C | snv | 0.44 | 1 | ||||
rs17088512 | 13 | 71832596 | intron variant | A/C | snv | 9.2E-02 | 1 | ||||
rs1780007 | 1 | 162778235 | intron variant | A/C | snv | 0.62 | 1 | ||||
rs2340721 | 1 | 161879595 | intron variant | A/C | snv | 0.49 | 1 | ||||
rs2494033 | 1 | 158698252 | upstream gene variant | A/C | snv | 0.14 | 1 | ||||
rs2684866 | 1 | 162756491 | intron variant | A/C | snv | 0.61 | 1 | ||||
rs35990176 | 21 | 43052008 | downstream gene variant | A/C | snv | 1 | |||||
rs3747869 | 10 | 71760875 | missense variant | A/C | snv | 0.88 | 0.90 | 1 | |||
rs4281320 | 1 | 26147948 | regulatory region variant | A/C | snv | 0.14 | 1 | ||||
rs59667935 | 22 | 17427131 | intron variant | A/C | snv | 0.15 | 1 |