| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121918455 | 0.695 | 0.440 | 12 | 112477720 | missense variant | A/C;G | snv | 31 | |||
| rs104894369 | 0.807 | 0.080 | 12 | 110914287 | missense variant | C/A;T | snv | 10 | |||
| rs35049558 | 0.851 | 0.040 | 12 | 110914287 | frameshift variant | -/CT | ins | 8.0E-06 | 8 | ||
| rs267607124 | 0.807 | 0.080 | 3 | 52451410 | missense variant | G/A;C;T | snv | 4.0E-05; 4.0E-06; 1.3E-04 | 6 | ||
| rs104894368 | 0.882 | 0.080 | 12 | 110919133 | stop gained | C/A;G;T | snv | 4.0E-06; 8.0E-06; 2.0E-05 | 4 | ||
| rs267607125 | 0.851 | 0.080 | 3 | 52453993 | missense variant | G/A | snv | 7.0E-06 | 4 | ||
| rs200754249 | 0.851 | 0.080 | 1 | 201368212 | missense variant | G/A;T | snv | 4.5E-04; 4.0E-06 | 4 | ||
| rs770640091 | 0.925 | 0.040 | 19 | 55157297 | missense variant | G/A | snv | 4.1E-06 | 2 | ||
| rs141754300 | 0.925 | 0.040 | 1 | 201364349 | missense variant | C/A | snv | 8.0E-06 | 2 | ||
| rs970498944 | 0.925 | 0.040 | 1 | 201373235 | missense variant | A/G | snv | 7.0E-06 | 2 | ||
| rs1407821871 | 1.000 | 18 | 3253269 | missense variant | A/G | snv | 4.0E-06 | 1 |