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 | |||
rs1057519770 | 0.882 | 0.160 | 19 | 17843825 | missense variant | A/G | snv | 3 | |||
rs201283129 | 0.882 | 0.160 | 19 | 17838329 | missense variant | C/A;G | snv | 2.0E-05 | 3 | ||
rs758959409 | 0.882 | 0.160 | 19 | 17835160 | missense variant | C/A;T | snv | 4.0E-06 | 3 |