| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1418810723 | 0.851 | 0.080 | 2 | 215409981 | missense variant | A/T | snv | 8.0E-06 | 9 | ||
| rs1250248 | 1.000 | 0.040 | 2 | 215422370 | intron variant | A/G | snv | 0.77 | 2 | ||
| rs1277989297 | 0.925 | 0.200 | 2 | 215428270 | stop gained | G/A | snv | 2 | |||
| rs777763524 | 1.000 | 0.040 | 2 | 215431961 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs757231578 | 1.000 | 0.080 | 2 | 215433387 | missense variant | A/C;T | snv | 2.8E-05 | 1 | ||
| rs530514393 | 1.000 | 0.080 | 2 | 215408367 | missense variant | T/A;C | snv | 2.2E-04; 4.0E-06 | 1 | ||
| rs80101897 | 1.000 | 0.080 | 2 | 215399334 | missense variant | T/C | snv | 4.0E-06 | 2.1E-05 | 1 | |
| rs370103949 | 1.000 | 0.120 | 2 | 215406438 | missense variant | G/A;T | snv | 2.0E-05; 4.0E-06 | 1 | ||
| rs1224741906 | 1.000 | 0.120 | 2 | 215408182 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs6725958 | 1.000 | 0.040 | 2 | 215397898 | intron variant | A/C | snv | 0.61 | 0.61 | 1 | |
| rs940739 | 1.000 | 0.040 | 2 | 215391428 | intron variant | T/A | snv | 0.32 | 1 | ||
| rs1553667072 | 0.882 | 0.200 | 2 | 215433372 | missense variant | A/G | snv | 1 | |||
| rs6707530 | 2 | 215375861 | intron variant | T/C;G | snv | 1 |