| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs797045032 | 0.827 | 0.280 | 7 | 143321720 | missense variant | GG/TC | mnv | 11 | |||
| rs80356696 | 0.851 | 0.120 | 7 | 143342001 | missense variant | A/G;T | snv | 4 | |||
| rs757109632 | 0.882 | 0.120 | 7 | 143324468 | missense variant | T/C | snv | 2.1E-05 | 3 | ||
| rs1554436419 | 0.925 | 0.120 | 7 | 143330816 | stop gained | CG/TA | mnv | 2 | |||
| rs1554436799 | 0.925 | 0.120 | 7 | 143332431 | stop gained | T/A | snv | 2 | |||
| rs1563084597 | 0.925 | 0.120 | 7 | 143341990 | frameshift variant | AT/- | del | 2 | |||
| rs201894078 | 0.925 | 0.120 | 7 | 143342451 | stop gained | C/T | snv | 1.4E-05 | 2 | ||
| rs759761559 | 0.925 | 0.120 | 7 | 143331264 | stop gained | C/T | snv | 2 | |||
| rs780534566 | 0.925 | 0.120 | 7 | 143350577 | frameshift variant | CT/- | del | 2 | |||
| rs1279658001 | 1.000 | 0.120 | 7 | 143332487 | missense variant | A/C | snv | 1.4E-05 | 1 | ||
| rs1554434400 | 1.000 | 0.120 | 7 | 143319794 | stop gained | C/T | snv | 1 | |||
| rs1554434794 | 1.000 | 0.120 | 7 | 143321399 | frameshift variant | C/- | delins | 1 | |||
| rs1554438574 | 1.000 | 0.120 | 7 | 143342492 | frameshift variant | G/- | delins | 1 | |||
| rs1554439817 | 1.000 | 0.120 | 7 | 143350387 | stop gained | C/T | snv | 1 | |||
| rs1554439879 | 1.000 | 0.120 | 7 | 143350623 | missense variant | G/A | snv | 1 | |||
| rs1563078827 | 1.000 | 0.120 | 7 | 143330898 | splice donor variant | G/A | snv | 1 | |||
| rs755433272 | 1.000 | 0.120 | 7 | 143350592 | missense variant | G/A;C | snv | 4.0E-06; 8.0E-06 | 1 | ||
| rs121912807 | 1.000 | 0.120 | 7 | 143339534 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs771532474 | 1.000 | 0.120 | 7 | 143321411 | missense variant | G/C | snv | 4.0E-06 | 1 | ||
| rs529377088 | 0.925 | 0.120 | 7 | 143320663 | splice acceptor variant | G/A | snv | 4.0E-06 | 2 | ||
| rs376026619 | 1.000 | 0.120 | 7 | 143332829 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-05 | 1 | ||
| rs80356702 | 0.882 | 0.120 | 7 | 143330868 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 9 | |
| rs80356692 | 0.882 | 0.120 | 7 | 143330855 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 3 | |
| rs777685454 | 1.000 | 0.120 | 7 | 143341952 | missense variant | G/A;C | snv | 2.4E-05; 4.0E-06 | 1 | ||
| rs121912805 | 1.000 | 0.120 | 7 | 143330789 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 |