| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121912745 | 0.807 | 0.200 | 17 | 44255708 | missense variant | G/A;T | snv | 9 | |||
| rs121912748 | 0.790 | 0.200 | 17 | 44253327 | missense variant | C/T | snv | 4.0E-05 | 2.1E-05 | 9 | |
| rs121912753 | 0.827 | 0.200 | 17 | 44251583 | missense variant | A/G | snv | 5 | |||
| rs121912754 | 0.882 | 0.200 | 17 | 44255292 | missense variant | C/G;T | snv | 3 | |||
| rs769664228 | 1.000 | 0.080 | 17 | 44258043 | inframe deletion | GGCAGCCAGGACCTGGGGGCTGAATGC/- | delins | 4.8E-05 | 4.2E-05 | 1 |