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 | |
rs121434444 | 0.882 | 0.160 | 12 | 57569648 | missense variant | C/T | snv | 2.8E-05 | 7.0E-06 | 4 | |
rs1471980111 | 6 | 38737948 | missense variant | G/A | snv | 4.1E-06 | 7.0E-06 | 1 | |||
rs1258159645 | 0.630 | 0.600 | 16 | 69711128 | missense variant | G/A | snv | 7.0E-06 | 37 | ||
rs1805032 | 1.000 | 0.040 | 2 | 151839238 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs80358261 | 0.925 | 0.160 | 14 | 74486404 | missense variant | C/T | snv | 1.7E-05 | 1.4E-05 | 3 | |
rs1280914556 | 1 | 32014269 | missense variant | A/G | snv | 2.1E-05 | 2 | ||||
rs28939711 | 0.851 | 0.120 | 10 | 99724057 | missense variant | G/A | snv | 3.2E-05 | 3.5E-05 | 5 | |
rs121908345 | 0.827 | 0.240 | 22 | 50080391 | missense variant | G/A | snv | 1.3E-04 | 6.3E-05 | 6 | |
rs1800014 | 0.776 | 0.200 | 20 | 4699875 | missense variant | G/A | snv | 8.0E-03 | 2.2E-03 | 11 | |
rs12252 | 0.695 | 0.240 | 11 | 320772 | splice region variant | A/G | snv | 0.13 | 0.13 | 23 | |
rs1801252 | 0.724 | 0.320 | 10 | 114044277 | missense variant | A/G | snv | 0.15 | 0.17 | 17 | |
rs1800566 | 0.576 | 0.680 | 16 | 69711242 | missense variant | G/A | snv | 0.25 | 0.21 | 59 | |
rs13963 | 3 | 45035631 | missense variant | G/A | snv | 0.49 | 0.43 | 1 |