| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs111854391 | 0.716 | 0.280 | 9 | 99138006 | stop gained | C/A;T | snv | 4.0E-06 | 18 | ||
| rs111426349 | 0.882 | 0.120 | 9 | 99149252 | missense variant | C/A;T | snv | 4.0E-06 | 4 | ||
| rs113605875 | 0.882 | 0.120 | 9 | 99149253 | missense variant | G/A;C;T | snv | 3 | |||
| rs387906697 | 1.000 | 9 | 99146594 | stop gained | C/T | snv | 2 | ||||
| rs760079636 | 1.000 | 0.120 | 9 | 99142664 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs863223829 | 1.000 | 0.120 | 9 | 99137962 | inframe deletion | AAG/- | delins | 1 | |||
| rs1554701911 | 1.000 | 0.120 | 9 | 99144816 | missense variant | G/T | snv | 1 | |||
| rs730880223 | 1.000 | 0.120 | 9 | 99149237 | missense variant | A/G | snv | 1 | |||
| rs886038919 | 1.000 | 0.120 | 9 | 99138041 | missense variant | A/G | snv | 1 | |||
| rs587776866 | 9 | 99142534 | splice acceptor variant | A/C | snv | 1 | |||||
| rs121918711 | 1.000 | 0.120 | 9 | 99146553 | missense variant | A/G | snv | 1 | |||
| rs1554701914 | 1.000 | 0.120 | 9 | 99144819 | missense variant | T/C | snv | 1 | |||
| rs727503470 | 1.000 | 0.120 | 9 | 99137924 | missense variant | G/A;T | snv | 1 | |||
| rs121918712 | 1.000 | 0.120 | 9 | 99137883 | missense variant | C/T | snv | 1 | |||
| rs121918710 | 1.000 | 0.120 | 9 | 99142683 | missense variant | T/G | snv | 1 | |||
| rs121918713 | 1.000 | 0.120 | 9 | 99132686 | missense variant | G/T | snv | 1.2E-05 | 1 | ||
| rs1564161224 | 1.000 | 9 | 99137859 | missense variant | G/A | snv | 1 | ||||
| rs1060502040 | 1.000 | 9 | 99132634 | stop gained | C/T | snv | 1 | ||||
| rs1057524497 | 1.000 | 9 | 99138017 | stop gained | G/A;T | snv | 1 | ||||
| rs1554701881 | 1.000 | 9 | 99144730 | splice acceptor variant | A/C;G | snv | 1 | ||||
| rs1554700672 | 1.000 | 9 | 99138065 | stop gained | G/T | snv | 1 | ||||
| rs886039176 | 1.000 | 9 | 99149250 | missense variant | T/C;G | snv | 1 | ||||
| rs1554702262 | 1.000 | 9 | 99146610 | splice donor variant | G/A | snv | 1 | ||||
| rs1554702463 | 1.000 | 9 | 99147701 | missense variant | G/C | snv | 1 | ||||
| rs863223832 | 1.000 | 9 | 99142590 | missense variant | C/A;T | snv | 1 |