Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs2910164 | 0.447 | 0.880 | 5 | 160485411 | mature miRNA variant | C/G | snv | 0.71; 4.1E-06 | 0.70 | 193 | |
rs1048943 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 88 | |
rs2274223 | 0.620 | 0.400 | 10 | 94306584 | missense variant | A/G | snv | 0.28 | 0.31 | 40 | |
rs2241880 | 0.627 | 0.600 | 2 | 233274722 | missense variant | A/G | snv | 0.45 | 0.44 | 37 | |
rs1864183 | 0.742 | 0.240 | 5 | 82253397 | missense variant | C/T | snv | 0.52 | 0.40 | 12 | |
rs3759601 | 0.790 | 0.240 | 14 | 96311131 | missense variant | G/C | snv | 0.36 | 0.32 | 7 | |
rs2238135 | 0.882 | 0.160 | 12 | 47884407 | intron variant | C/G | snv | 0.26 | 4 | ||
rs7834169 | 0.925 | 0.120 | 8 | 27052774 | upstream gene variant | C/G | snv | 0.16 | 3 | ||
rs1816158 | 0.925 | 0.200 | 11 | 122155752 | intron variant | C/A;T | snv | 3 | |||
rs1373756 | 1.000 | 0.120 | 18 | 52259936 | intergenic variant | C/T | snv | 0.24 | 2 | ||
rs221236 | 1.000 | 0.120 | 7 | 157529938 | downstream gene variant | G/A | snv | 0.96 | 2 | ||
rs16914640 | 1.000 | 0.120 | 12 | 9669791 | missense variant | C/G;T | snv | 0.14; 4.0E-06 | 2 | ||
rs221636 | 1.000 | 0.120 | 6 | 105082089 | 3 prime UTR variant | T/A | snv | 0.82 | 2 | ||
rs1271546630 | 1.000 | 0.120 | 17 | 58277848 | missense variant | G/A;C | snv | 2 |