| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1232369409 | 1.000 | 0.120 | 4 | 88008244 | frameshift variant | G/- | delins | 7.0E-06 | 1 | ||
| rs1391596181 | 1.000 | 0.120 | 4 | 88046647 | stop gained | T/A;C | snv | 4.0E-06 | 1 | ||
| rs1392093609 | 1.000 | 0.120 | 4 | 88007759 | missense variant | C/T | snv | 1 | |||
| rs1553926509 | 1.000 | 0.120 | 4 | 88052018 | frameshift variant | TA/- | delins | 1 | |||
| rs1553926905 | 1.000 | 0.120 | 4 | 88056143 | stop gained | C/T | snv | 1 | |||
| rs1553927080 | 1.000 | 0.120 | 4 | 88058104 | splice donor variant | G/A | snv | 1 | |||
| rs1560592253 | 1.000 | 0.120 | 4 | 88008174 | frameshift variant | G/- | delins | 1 | |||
| rs749004212 | 1.000 | 0.120 | 4 | 88038365 | stop gained | C/T | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs1487813753 | 1.000 | 0.120 | 10 | 100293336 | missense variant | T/C;G | snv | 8.0E-06 | 1 | ||
| rs746231889 | 1.000 | 0.120 | 19 | 11447152 | missense variant | C/A;G;T | snv | 4.0E-06; 1.9E-04 | 1 |