Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs143396368 | 0.807 | 0.200 | 9 | 69072623 | missense variant | G/A;C | snv | 3.2E-05; 8.0E-06 | 7 | ||
| rs104894107 | 0.882 | 0.160 | 9 | 69064942 | missense variant | G/C;T | snv | 3.6E-05; 2.8E-05 | 6 | ||
| rs142157346 | 0.882 | 0.160 | 9 | 69053240 | missense variant | G/T | snv | 4 | |||
| rs104894105 | 0.925 | 0.120 | 9 | 69053193 | stop gained | T/C;G | snv | 1.2E-05 | 2 | ||
| rs104894106 | 0.925 | 0.120 | 9 | 69065013 | missense variant | A/G;T | snv | 4.0E-06 | 2 | ||
| rs138034837 | 0.925 | 0.120 | 9 | 69072622 | missense variant | C/T | snv | 2 | |||
| rs138471431 | 0.925 | 0.120 | 9 | 69065016 | missense variant | T/C | snv | 2 | |||
| rs104894108 | 1.000 | 0.120 | 9 | 69035785 | start lost | G/A;T | snv | 9.1E-06 | 1 | ||
| rs139616452 | 1.000 | 0.120 | 9 | 69072673 | missense variant | C/T | snv | 1 | |||
| rs140987490 | 1.000 | 0.120 | 9 | 69064936 | splice acceptor variant | A/G | snv | 1 | |||
| rs141935559 | 1.000 | 0.120 | 9 | 69035936 | frameshift variant | C/-;CC | delins | 1 | |||
| rs144104124 | 1.000 | 0.120 | 9 | 69072722 | missense variant | T/G | snv | 1 | |||
| rs146818694 | 1.000 | 0.120 | 9 | 69064991 | missense variant | C/G | snv | 1 | |||
| rs148443992 | 1.000 | 0.120 | 9 | 69072686 | missense variant | T/G | snv | 1 | |||
| rs56214919 | 1.000 | 0.120 | 9 | 69072646 | missense variant | T/G | snv | 1 | |||
| rs886037630 | 1.000 | 0.120 | 9 | 69053247 | protein altering variant | ATGTCT/TACACCTTGAGGACA | delins | 1 |