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 | |||
rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
rs72470545 | 0.807 | 0.280 | 2 | 74532698 | missense variant | G/A | snv | 4.0E-03 | 2.5E-03 | 6 | |
rs786201031 | 0.925 | 0.280 | 22 | 24412690 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 2 | |
rs1555895466 | 1.000 | 0.200 | 22 | 19761162 | stop gained | A/T | snv | 1 | |||
rs41298838 | 1.000 | 0.200 | 22 | 19765921 | missense variant | G/A;T | snv | 5.2E-03 | 1 |