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 | |||
rs397516835 | 0.925 | 0.080 | 1 | 17024040 | missense variant | C/G;T | snv | 4 | |||
rs80338846 | 0.882 | 0.080 | 11 | 112088981 | missense variant | T/C | snv | 3 | |||
rs1393298155 | 1.000 | 0.040 | 5 | 225998 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 1 |