Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28933979 | 0.587 | 0.600 | 18 | 31592974 | missense variant | G/A;C | snv | 1.0E-04 | 70 | ||
rs121909211 | 0.724 | 0.200 | 5 | 136046407 | missense variant | G/A;T | snv | 4.0E-05 | 15 | ||
rs63750579 | 0.742 | 0.280 | 21 | 25891856 | missense variant | C/G;T | snv | 13 | |||
rs74315409 | 0.742 | 0.240 | 20 | 4699915 | missense variant | T/G | snv | 6.0E-05 | 2.1E-05 | 13 | |
rs121918097 | 0.790 | 0.280 | 18 | 31595137 | missense variant | G/A | snv | 10 | |||
rs28939068 | 0.790 | 0.200 | 20 | 23635330 | missense variant | A/T | snv | 9 | |||
rs121913547 | 0.807 | 0.200 | 12 | 69350192 | missense variant | T/C | snv | 7 | |||
rs1052006472 | 0.827 | 0.200 | 5 | 136060907 | missense variant | A/G | snv | 5 | |||
rs753737986 | 0.925 | 0.200 | 21 | 26111983 | missense variant | T/A | snv | 4.0E-06 | 2 | ||
rs1434458385 | 1.000 | 0.040 | 1 | 58576708 | missense variant | C/A | snv | 7.0E-06 | 1 |