| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909233 | 1.000 | 0.040 | 10 | 87864524 | missense variant | G/A | snv | 1 | |||
| rs786204931 | 0.925 | 0.120 | 10 | 87933126 | missense variant | C/G;T | snv | 1 | |||
| rs121909237 | 1.000 | 0.040 | 10 | 87933121 | missense variant | C/G | snv | 1 | |||
| rs397514559 | 0.925 | 0.240 | 10 | 87952125 | missense variant | C/A | snv | 1 | |||
| rs121909239 | 0.925 | 0.240 | 10 | 87957973 | missense variant | A/G;T | snv | 1 | |||
| rs121909240 | 0.925 | 0.240 | 10 | 87957940 | missense variant | T/C | snv | 1 | |||
| rs121909238 | 0.925 | 0.240 | 10 | 87933037 | missense variant | A/C;G | snv | 1 | |||
| rs397514560 | 0.925 | 0.240 | 10 | 87933151 | missense variant | C/G;T | snv | 1 | |||
| rs121909235 | 0.851 | 0.240 | 10 | 87957919 | missense variant | G/A | snv | 1 |