| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267606746 | 1.000 | 0.160 | 21 | 45989120 | missense variant | G/A | snv | 1 | |||
| rs267606749 | 1.000 | 0.160 | 21 | 46121590 | missense variant | G/A | snv | 2.4E-05 | 4.9E-05 | 1 | |
| rs387906607 | 1.000 | 0.160 | 21 | 46125518 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs387906608 | 1.000 | 0.160 | 21 | 46132118 | missense variant | C/A;G;T | snv | 5.2E-06; 2.1E-05 | 1 | ||
| rs398122821 | 1.000 | 0.160 | 21 | 46125501 | inframe deletion | TCATCG/- | delins | 1 | |||
| rs748035948 | 1.000 | 0.160 | 21 | 46125265 | splice acceptor variant | G/T | snv | 1 | |||
| rs75120695 | 1.000 | 0.160 | 21 | 46126166 | missense variant | G/A;C | snv | 4.4E-03 | 1 | ||
| rs797044457 | 1.000 | 0.160 | 21 | 45989135 | frameshift variant | C/- | delins | 1 | |||
| rs797044458 | 1.000 | 0.160 | 21 | 45997703 | frameshift variant | G/- | del | 1 |