| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11554290 | 0.583 | 0.600 | 1 | 114713908 | missense variant | T/A;C;G | snv | 4 | |||
| rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 3 | ||
| rs121913487 | 0.925 | 0.120 | 13 | 28018503 | missense variant | A/C;T | snv | 2 | |||
| rs121913615 | 0.683 | 0.240 | 1 | 43349338 | missense variant | G/C;T | snv | 8.0E-06 | 2 | ||
| rs1801265 | 0.763 | 0.280 | 1 | 97883329 | missense variant | A/G | snv | 0.28 | 1 | ||
| rs121909646 | 0.882 | 0.120 | 13 | 28018504 | missense variant | T/A;G | snv | 1 | |||
| rs121913232 | 0.925 | 0.120 | 13 | 28018500 | missense variant | G/C | snv | 1 | |||
| rs121913488 | 0.807 | 0.120 | 13 | 28018505 | missense variant | C/A;G;T | snv | 1 | |||
| rs398123063 | 0.925 | 0.120 | 9 | 37002705 | missense variant | C/T | snv | 1 | |||
| rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 1 | |
| rs61754966 | 0.701 | 0.280 | 8 | 89978293 | missense variant | T/C;G | snv | 1.2E-03 | 1 | ||
| rs397507520 | 0.658 | 0.520 | 12 | 112453279 | missense variant | G/C;T | snv | 1 | |||
| rs1478147351 | 1.000 | 0.120 | 3 | 47101485 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs186148199 | 1.000 | 0.120 | 3 | 47123837 | missense variant | C/T | snv | 8.9E-05 | 3.5E-05 | 1 | |
| rs188887061 | 1.000 | 0.120 | 3 | 47122353 | missense variant | C/T | snv | 4.2E-04 | 7.0E-05 | 1 | |
| rs540476365 | 1.000 | 0.120 | 3 | 47121125 | missense variant | T/C | snv | 1 | |||
| rs780963440 | 1.000 | 0.120 | 3 | 47123960 | missense variant | G/A;C | snv | 5.0E-05; 1.3E-05 | 1 |