| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267606749 | 1.000 | 0.160 | 21 | 46121590 | missense variant | G/A | snv | 2.4E-05 | 4.9E-05 | 1 | |
| rs121912937 | 1.000 | 0.160 | 21 | 46001981 | stop gained | C/G;T | snv | 2.5E-05 | 1 | ||
| rs150168522 | 0.925 | 0.160 | 21 | 46132367 | missense variant | G/A;C | snv | 4.9E-05; 2.9E-05 | 4 | ||
| rs398124119 | 0.882 | 0.160 | 2 | 237395121 | stop gained | G/A | snv | 4.4E-05 | 2.8E-05 | 3 | |
| rs778940391 | 1.000 | 0.160 | 2 | 237367167 | missense variant | C/T | snv | 1.6E-04 | 9.1E-05 | 1 | |
| rs137964147 | 1.000 | 0.160 | 21 | 45982738 | missense variant | C/T | snv | 5.5E-04 | 5.7E-04 | 1 | |
| rs112638391 | 1.000 | 0.160 | 2 | 237374900 | missense variant | C/T | snv | 3.0E-03 | 3.0E-03 | 1 | |
| rs75120695 | 1.000 | 0.160 | 21 | 46126166 | missense variant | G/A;C | snv | 4.4E-03 | 1 | ||
| rs80272723 | 1.000 | 0.160 | 2 | 237371833 | missense variant | C/A;T | snv | 1.0E-02 | 1 |