Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs13405728 | 0.790 | 0.200 | 2 | 48751020 | intron variant | A/G | snv | 0.15 | 8 | ||
rs2479106 | 0.851 | 0.120 | 9 | 123762933 | intron variant | A/G | snv | 0.44 | 4 |