| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267607102 | 0.851 | 0.120 | 1 | 11022196 | missense variant | A/G | snv | 5 | |||
| rs28933979 | 0.587 | 0.600 | 18 | 31592974 | missense variant | G/A;C | snv | 1.0E-04 | 70 | ||
| rs28939711 | 0.851 | 0.120 | 10 | 99724057 | missense variant | G/A | snv | 3.2E-05 | 3.5E-05 | 5 | |
| rs374651285 | 4 | 73406645 | missense variant | G/A | snv | 1 | |||||
| rs397514662 | 0.882 | 0.120 | 10 | 99716419 | missense variant | A/C;G | snv | 1.2E-05 | 4 | ||
| rs398122370 | 0.925 | 0.160 | 20 | 4699851 | missense variant | G/C | snv | 4 | |||
| rs587777162 | 0.925 | 0.040 | 20 | 63495972 | missense variant | C/T | snv | 5 | |||
| rs62643364 | 0.851 | 0.160 | 20 | 4699466 | synonymous variant | A/G;T | snv | 4.0E-06; 1.4E-04 | 7 | ||
| rs74315322 | 1.000 | 0.040 | 1 | 154275165 | stop gained | C/T | snv | 3.6E-05 | 3 | ||
| rs749191312 | 1.000 | 0.080 | 20 | 18497075 | synonymous variant | C/T | snv | 4.0E-06 | 2 | ||
| rs756915170 | 19 | 49909654 | missense variant | T/C | snv | 4.0E-06 | 2 | ||||
| rs771884087 | 1.000 | 0.080 | 20 | 45253726 | synonymous variant | T/C | snv | 2 | |||
| rs80356717 | 0.851 | 0.120 | 1 | 11018836 | missense variant | A/G | snv | 5 | |||
| rs80358261 | 0.925 | 0.160 | 14 | 74486404 | missense variant | C/T | snv | 1.7E-05 | 1.4E-05 | 3 |