Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17655 | 0.597 | 0.560 | 13 | 102875652 | missense variant | G/C | snv | 0.28 | 0.30 | 52 | |
rs9514828 | 0.752 | 0.440 | 13 | 108269025 | intron variant | C/T | snv | 0.35 | 12 | ||
rs145036301 | 0.851 | 0.120 | 19 | 11513899 | missense variant | A/G | snv | 2.7E-03 | 9.4E-04 | 5 | |
rs2069812 | 0.851 | 0.240 | 5 | 132544224 | intron variant | A/G | snv | 0.54 | 5 | ||
rs1442744764 | 1.000 | 0.120 | 9 | 136496490 | missense variant | G/A | snv | 4.2E-06 | 1 | ||
rs1800896 | 0.507 | 0.800 | 1 | 206773552 | intron variant | T/C | snv | 0.41 | 113 | ||
rs1801195 | 0.776 | 0.240 | 8 | 31141764 | missense variant | G/A;T | snv | 8.0E-06; 0.45 | 0.46 | 8 | |
rs477145 | 1.000 | 0.120 | 21 | 31390097 | intron variant | C/A;T | snv | 4 | |||
rs1800629 | 0.472 | 0.920 | 6 | 31575254 | upstream gene variant | G/A | snv | 0.12 | 0.14 | 169 | |
rs745738344 | 0.653 | 0.600 | 6 | 31576786 | synonymous variant | G/A | snv | 1.6E-05 | 1.4E-05 | 28 | |
rs9808753 | 0.701 | 0.400 | 21 | 33415005 | missense variant | A/G | snv | 0.20 | 0.18 | 17 | |
rs1494555 | 0.790 | 0.120 | 5 | 35871088 | missense variant | G/A | snv | 0.64 | 0.72 | 8 | |
rs2835931 | 1.000 | 0.120 | 21 | 37749345 | intron variant | C/A;T | snv | 4 | |||
rs938448224 | 0.807 | 0.160 | 17 | 42207711 | missense variant | T/G | snv | 7.0E-06 | 7 | ||
rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 134 | ||
rs61733010 | 0.925 | 0.120 | 1 | 45561805 | missense variant | C/G;T | snv | 4.0E-06; 4.3E-04 | 1.9E-03 | 2 | |
rs731236 | 0.542 | 0.760 | 12 | 47844974 | synonymous variant | A/G | snv | 0.33 | 0.34 | 81 | |
rs753861648 | 1.000 | 0.120 | 19 | 54906742 | missense variant | G/C | snv | 4.0E-06 | 2 | ||
rs1048943 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 88 | |
rs753716491 | 1.000 | 0.120 | 9 | 77922196 | missense variant | T/A | snv | 2 | |||
rs758837678 | 0.925 | 0.120 | 8 | 90001503 | missense variant | C/T | snv | 2 | |||
rs752317734 | 0.851 | 0.120 | 8 | 90020913 | missense variant | T/C | snv | 4.9E-06 | 5 | ||
rs3742330 | 0.662 | 0.640 | 14 | 95087025 | 3 prime UTR variant | A/G | snv | 8.7E-02 | 24 | ||
rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 113 |