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 | |||
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
rs2479106 | 0.851 | 0.120 | 9 | 123762933 | intron variant | A/G | snv | 0.44 | 4 | ||
rs2476491 | 0.776 | 0.240 | 10 | 6053447 | intron variant | A/T | snv | 0.25 | 8 | ||
rs10795763 | 0.925 | 0.120 | 10 | 6054236 | intron variant | G/T | snv | 0.45 | 2 | ||
rs11256497 | 0.925 | 0.120 | 10 | 6045831 | intron variant | G/A | snv | 0.28 | 2 | ||
rs791587 | 0.925 | 0.120 | 10 | 6046736 | intron variant | A/G | snv | 0.51 | 2 | ||
rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 71 | ||
rs1057519945 | 0.776 | 0.200 | 12 | 132673703 | missense variant | C/A;T | snv | 12 | |||
rs1057519943 | 0.790 | 0.160 | 12 | 132676598 | missense variant | G/C;T | snv | 10 | |||
rs13405728 | 0.790 | 0.200 | 2 | 48751020 | intron variant | A/G | snv | 0.15 | 8 |