| 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 | |||
| rs121912751 | 0.882 | 0.200 | 17 | 44251241 | missense variant | G/T | snv | 7.2E-05 | 2.1E-05 | 4 | |
| rs121912754 | 0.882 | 0.200 | 17 | 44255292 | missense variant | C/G;T | snv | 3 | |||
| rs557128345 | 0.882 | 0.240 | 15 | 53615520 | stop gained | G/A | snv | 2.4E-05 | 7.0E-06 | 3 | |
| rs10258719 | 0.925 | 0.280 | 7 | 138771243 | missense variant | A/C;G;T | snv | 0.69 | 2 | ||
| rs1376457227 | 0.925 | 0.200 | 15 | 53665757 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
| rs768446132 | 0.925 | 0.200 | 15 | 53615684 | missense variant | A/T | snv | 8.1E-06 | 2 | ||
| rs1325804996 | 1.000 | 0.160 | 6 | 38786789 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs1238908071 | 1.000 | 0.160 | 10 | 69398764 | missense variant | A/G | snv | 1 | |||
| rs1335780263 | 1.000 | 0.160 | 12 | 48145569 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs121912744 | 1.000 | 0.160 | 17 | 44255707 | missense variant | C/T | snv | 1 | |||
| rs121912746 | 1.000 | 0.160 | 17 | 44255259 | missense variant | G/A | snv | 1 | |||
| rs765891978 | 1.000 | 0.160 | 17 | 44258106 | missense variant | G/A;T | snv | 4.0E-05; 4.0E-06 | 1 | ||
| rs878853002 | 1.000 | 0.160 | 17 | 44255272 | missense variant | C/T | snv | 1 | |||
| rs999716 | 1.000 | 0.160 | 17 | 44262056 | non coding transcript exon variant | C/G;T | snv | 1 | |||
| rs1295540039 | 1.000 | 0.160 | 3 | 27390094 | missense variant | C/T | snv | 8.2E-06 | 1.4E-05 | 1 |