| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs869025615 | 1.000 | 0.120 | 3 | 10142009 | frameshift variant | G/-;GG | delins | 2 | |||
| rs730882037 | 3 | 10142026 | frameshift variant | G/- | delins | 1 | |||||
| rs104893826 | 0.882 | 0.200 | 3 | 10142038 | missense variant | G/A;C | snv | 4 | |||
| rs730882031 | 1.000 | 0.120 | 3 | 10142039 | frameshift variant | C/- | del | 2 | |||
| rs5030802 | 1.000 | 0.120 | 3 | 10142055 | stop gained | G/A;T | snv | 4.4E-06 | 2 | ||
| rs869025618 | 1.000 | 0.120 | 3 | 10142061 | missense variant | T/C | snv | 2 | |||
| rs730882039 | 3 | 10142066 | frameshift variant | GG/- | del | 1 | |||||
| rs869025621 | 0.882 | 0.240 | 3 | 10142079 | missense variant | A/C;G;T | snv | 4 | |||
| rs5030804 | 0.925 | 0.160 | 3 | 10142080 | missense variant | A/C;G;T | snv | 3 | |||
| rs786202787 | 1.000 | 0.120 | 3 | 10142085 | missense variant | A/C;G | snv | 2 | |||
| rs193922608 | 1.000 | 0.120 | 3 | 10142089 | missense variant | C/A;T | snv | 4.3E-06; 4.3E-06 | 2 | ||
| rs5030827 | 0.882 | 0.200 | 3 | 10142097 | missense variant | G/A;C;T | snv | 4.4E-06 | 4 | ||
| rs398123481 | 1.000 | 0.120 | 3 | 10142103 | missense variant | C/G;T | snv | 2 | |||
| rs730882034 | 0.925 | 0.160 | 3 | 10142104 | missense variant | C/G;T | snv | 3 | |||
| rs1131690960 | 3 | 10142109 | protein altering variant | -/GGC | delins | 1 | |||||
| rs119103277 | 0.925 | 0.160 | 3 | 10142110 | stop gained | G/A;C | snv | 3 | |||
| rs869025622 | 0.925 | 0.160 | 3 | 10142111 | missense variant | G/C;T | snv | 3 | |||
| rs5030807 | 0.851 | 0.320 | 3 | 10142113 | missense variant | T/A;C | snv | 5 | |||
| rs1131690964 | 1.000 | 0.120 | 3 | 10142124 | frameshift variant | G/- | delins | 2 | |||
| rs5030829 | 1.000 | 0.120 | 3 | 10142127 | stop gained | G/A;T | snv | 4.5E-06 | 2 | ||
| rs1131690959 | 3 | 10142133 | stop gained | C/T | snv | 1 | |||||
| rs5030809 | 0.776 | 0.320 | 3 | 10142139 | missense variant | T/C | snv | 1.3E-05 | 10 | ||
| rs193922609 | 1.000 | 0.120 | 3 | 10142167 | missense variant | G/A;C | snv | 2 | |||
| rs869025631 | 1.000 | 0.120 | 3 | 10142179 | missense variant | G/A;T | snv | 2 | |||
| rs765978945 | 1.000 | 0.120 | 3 | 10142180 | missense variant | C/G;T | snv | 4.5E-06 | 2 |