Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs266729 | 0.637 | 0.560 | 3 | 186841685 | upstream gene variant | C/A;G;T | snv | 37 | |||
rs486907 | 0.667 | 0.360 | 1 | 182585422 | missense variant | C/T | snv | 0.31 | 0.28 | 32 | |
rs138213197 | 0.701 | 0.240 | 17 | 48728343 | missense variant | C/T | snv | 1.8E-03 | 1.6E-03 | 24 | |
rs182052 | 0.701 | 0.440 | 3 | 186842993 | intron variant | G/A | snv | 0.38 | 19 | ||
rs1057519912 | 0.776 | 0.200 | X | 71129408 | missense variant | C/G;T | snv | 11 | |||
rs137852578 | 0.827 | 0.080 | X | 67723710 | missense variant | A/G | snv | 10 | |||
rs1057519864 | 0.851 | 0.080 | X | 67723707 | missense variant | T/C | snv | 8 | |||
rs976306779 | 0.851 | 0.080 | X | 67545492 | missense variant | C/A;T | snv | 6.6E-06 | 8 | ||
rs1512268 | 0.851 | 0.160 | 8 | 23668950 | intergenic variant | T/C | snv | 0.50 | 6 | ||
rs1571801 | 0.827 | 0.120 | 9 | 121665094 | intron variant | G/T | snv | 0.21 | 6 | ||
rs137852581 | 0.882 | 0.080 | X | 67723701 | missense variant | C/T | snv | 5 | |||
rs1060501201 | 0.925 | 0.080 | 17 | 7674190 | missense variant | T/C;G | snv | 4 | |||
rs1197734477 | 0.925 | 0.080 | 10 | 87961012 | missense variant | A/G | snv | 4 | |||
rs339331 | 0.882 | 0.080 | 6 | 116888889 | intron variant | T/C | snv | 0.28 | 4 | ||
rs375118292 | 0.925 | 0.080 | 2 | 224506080 | missense variant | T/A;C | snv | 2.0E-05 | 3 | ||
rs727502792 | 0.925 | 0.080 | 17 | 49601958 | missense variant | T/A | snv | 3 | |||
rs746001963 | 0.925 | 0.080 | 21 | 38383659 | missense variant | A/T | snv | 4.0E-06 | 3 |