Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1557043622 | 0.695 | 0.400 | X | 48909843 | missense variant | C/A | snv | 46 | |||
rs387906799 | 0.742 | 0.200 | 2 | 240788118 | missense variant | G/A | snv | 17 | |||
rs267607093 | 0.851 | 0.160 | 4 | 55359444 | stop gained | G/A | snv | 4.0E-06 | 14 | ||
rs758022116 | 0.790 | 0.280 | 20 | 38535152 | missense variant | G/T | snv | 4.0E-06 | 13 | ||
rs1566785990 | 0.851 | 0.120 | 14 | 77026534 | missense variant | A/G | snv | 12 | |||
rs35135520 | 0.827 | 0.200 | 19 | 39480879 | stop gained | C/A;G;T | snv | 3.1E-03; 4.6E-06 | 12 | ||
rs776019250 | 0.827 | 0.200 | 19 | 39482885 | stop gained | G/C;T | snv | 4.0E-06 | 12 |