Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137854618 | 0.742 | 0.120 | 3 | 38566426 | missense variant | C/A;T | snv | 8.0E-06 | 15 | ||
rs104893875 | 0.742 | 0.120 | 4 | 89828170 | missense variant | C/T | snv | 4.0E-06 | 13 | ||
rs121912633 | 0.790 | 0.240 | 12 | 109792396 | missense variant | C/A;T | snv | 4.0E-06 | 10 | ||
rs80338958 | 0.790 | 0.200 | 17 | 63945614 | missense variant | C/A;T | snv | 1.6E-05; 5.6E-05 | 9 | ||
rs786205753 | 0.925 | 0.080 | 12 | 2593255 | missense variant | G/A | snv | 3 | |||
rs778250646 | 0.925 | 0.080 | 21 | 26112008 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs1057521065 | 1.000 | 0.040 | 17 | 63968310 | missense variant | A/G | snv | 1 | |||
rs41261344 | 0.763 | 0.120 | 3 | 38575385 | missense variant | C/T | snv | 5.4E-03 | 2.2E-03 | 11 |