| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs55735910 | 1.000 | 0.040 | 8 | 47881444 | missense variant | G/A | snv | 1.4E-05 | 1 | ||
| rs267600891 | 1.000 | 0.040 | 6 | 166469882 | missense variant | C/T | snv | 1 | |||
| rs564777385 | 1.000 | 0.040 | 2 | 178800635 | missense variant | C/G;T | snv | 3.6E-05 | 1 | ||
| rs267599092 | 1.000 | 0.040 | 2 | 178779043 | missense variant | C/T | snv | 1 | |||
| rs1204056923 | 1.000 | 0.040 | 2 | 178590160 | missense variant | C/T | snv | 1.4E-05 | 1 | ||
| rs369098292 | 1.000 | 0.040 | 2 | 178572742 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs374713701 | 1.000 | 0.040 | 2 | 178593660 | missense variant | C/A;T | snv | 4.0E-06; 8.1E-06 | 1 | ||
| rs1458591077 | 1.000 | 0.040 | 2 | 178630352 | missense variant | C/T | snv | 1 | |||
| rs375422359 | 1.000 | 0.040 | 2 | 178563634 | missense variant | C/T | snv | 2.4E-05 | 3.5E-05 | 1 | |
| rs764005465 | 1.000 | 0.040 | 2 | 178572808 | missense variant | C/T | snv | 8.1E-06 | 1 | ||
| rs2228570 | 0.521 | 0.760 | 12 | 47879112 | start lost | A/C;G;T | snv | 0.63 | 1 |