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 | |||
rs1057519781 | 0.807 | 0.160 | 2 | 29209816 | missense variant | C/G | snv | 9 | |||
rs113994089 | 0.925 | 0.120 | 2 | 29220776 | missense variant | C/G;T | snv | 4 | |||
rs113994091 | 0.882 | 0.160 | 2 | 29222407 | missense variant | G/A;C | snv | 3.2E-05 | 4 | ||
rs201227909 | 0.925 | 0.160 | 14 | 104770839 | synonymous variant | T/C | snv | 2 | |||
rs1057519859 | 1.000 | 0.120 | 2 | 29222392 | missense variant | C/T | snv | 2 | |||
rs763830096 | 1.000 | 0.120 | 7 | 55157724 | synonymous variant | A/G | snv | 4.0E-06 | 1 | ||
rs1226137439 | 1.000 | 0.120 | 7 | 106868830 | synonymous variant | G/A | snv | 4.0E-06 | 1 | ||
rs863224686 | 1.000 | 0.120 | 17 | 7673716 | missense variant | C/G | snv | 1 |