Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2105903 | 1.000 | 0.040 | 6 | 32427879 | intergenic variant | A/T | snv | 0.14 | 3 | ||
rs227731 | 0.882 | 0.120 | 17 | 56695877 | intergenic variant | T/A;G | snv | 3 | |||
rs2290263 | 7 | 25847658 | intergenic variant | G/A | snv | 0.77 | 3 | ||||
rs2453533 | 1.000 | 0.080 | 15 | 45349027 | intergenic variant | C/A | snv | 0.56 | 3 | ||
rs267734 | 0.925 | 0.120 | 1 | 150979001 | upstream gene variant | T/C | snv | 0.14 | 3 | ||
rs3132374 | 1.000 | 0.040 | 6 | 28900717 | downstream gene variant | C/G | snv | 5.3E-02 | 3 | ||
rs34861762 | 1.000 | 0.080 | 8 | 23890907 | regulatory region variant | C/T | snv | 0.37 | 3 | ||
rs60307791 | 1.000 | 0.040 | 11 | 65767714 | intron variant | TT/-;T;TTT;TTTT | delins | 3 | |||
rs6465825 | 1.000 | 0.080 | 7 | 77787122 | downstream gene variant | T/C | snv | 0.41 | 3 | ||
rs7012637 | 8 | 9315699 | intron variant | G/A;C | snv | 3 | |||||
rs10277115 | 7 | 1245559 | regulatory region variant | A/T | snv | 0.57 | 2 | ||||
rs10840341 | 11 | 2095263 | intergenic variant | T/A;C | snv | 2 | |||||
rs115114609 | 1.000 | 0.080 | 5 | 88448197 | intron variant | G/A | snv | 3.4E-02 | 2 | ||
rs11604462 | 11 | 65784177 | upstream gene variant | G/A | snv | 0.30 | 2 | ||||
rs11742501 | 5 | 151727535 | upstream gene variant | T/C | snv | 0.29 | 2 | ||||
rs12458009 | 18 | 61683274 | intron variant | T/C;G | snv | 2 | |||||
rs12845465 | X | 8944553 | intergenic variant | T/C | snv | 1.5E-03 | 2 | ||||
rs143297173 | 6 | 55418058 | intergenic variant | A/C | snv | 6.7E-04 | 2 | ||||
rs1705694 | 8 | 23912105 | intergenic variant | A/C;G | snv | 0.50 | 2 | ||||
rs1813937 | 1.000 | 0.080 | 11 | 50509630 | intergenic variant | C/T | snv | 0.76 | 2 | ||
rs281380 | 19 | 48711213 | downstream gene variant | T/C | snv | 0.39 | 2 | ||||
rs35320690 | 3 | 136213652 | intergenic variant | T/C | snv | 0.20 | 2 | ||||
rs36071802 | 8 | 23858358 | upstream gene variant | T/A;C | snv | 2 | |||||
rs3758086 | 8 | 23857479 | upstream gene variant | G/A | snv | 0.37 | 2 | ||||
rs55703462 | 15 | 63103229 | intron variant | A/G | snv | 0.42 | 2 |