| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs769236847 | 0.807 | 0.200 | 7 | 97869011 | missense variant | C/T | snv | 4.0E-06 | 3.5E-05 | 8 | |
| rs948326794 | 1.000 | 7 | 97854653 | stop gained | C/A;G | snv | 1.4E-05 | 2 | |||
| rs1481539409 | 1.000 | 7 | 97859285 | frameshift variant | T/- | delins | 2 | ||||
| rs1554350554 | 1.000 | 7 | 97868955 | missense variant | G/T | snv | 1 | ||||
| rs1562817048 | 1.000 | 7 | 97859317 | stop gained | A/C | snv | 1 | ||||
| rs398122974 | 1.000 | 7 | 97852297 | missense variant | G/A | snv | 1.6E-05 | 1.4E-05 | 1 | ||
| rs398122975 | 1.000 | 7 | 97869140 | missense variant | G/A;T | snv | 2.4E-05; 1.2E-05 | 1 | |||
| rs797045306 | 1.000 | 7 | 97864333 | missense variant | T/A | snv | 1 | ||||
| rs148111963 | 1.000 | 7 | 97858901 | missense variant | A/G | snv | 4.0E-06 | 2.1E-05 | 1 | ||
| rs398122973 | 1.000 | 7 | 97855406 | missense variant | A/C | snv | 1 | ||||
| rs754043007 | 1.000 | 7 | 97853097 | missense variant | G/A | snv | 2.1E-05 | 7.0E-06 | 1 | ||
| rs780288372 | 1.000 | 7 | 97856689 | splice donor variant | C/T | snv | 4.1E-06 | 1 | |||
| rs797045307 | 1.000 | 7 | 97864268 | frameshift variant | C/- | del | 1 |