| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2070074 | 0.742 | 0.360 | 9 | 34649445 | missense variant | A/G | snv | 9.2E-02 | 7.4E-02 | 12 | |
| rs75391579 | 0.827 | 0.280 | 9 | 34648170 | missense variant | A/G | snv | 1.4E-03 | 1.9E-03 | 5 | |
| rs121908047 | 0.851 | 0.120 | 1 | 23798188 | missense variant | C/T | snv | 8.0E-06 | 1.4E-05 | 4 | |
| rs111033806 | 0.882 | 0.160 | 9 | 34649523 | stop gained | G/A;T | snv | 4 | |||
| rs137853859 | 0.882 | 0.120 | 1 | 23797718 | missense variant | G/A;T | snv | 7.2E-05; 8.0E-06 | 3 | ||
| rs137853860 | 0.882 | 0.120 | 1 | 23796777 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 3 | |
| rs137853861 | 0.882 | 0.120 | 1 | 23796234 | missense variant | C/T | snv | 2.0E-05 | 3 | ||
| rs28940882 | 0.882 | 0.120 | 1 | 23798199 | missense variant | C/T | snv | 3 | |||
| rs28940884 | 0.882 | 0.120 | 1 | 23796722 | missense variant | T/C | snv | 1.4E-03 | 5.8E-03 | 3 | |
| rs3180383 | 0.882 | 0.120 | 1 | 23796202 | missense variant | G/A;T | snv | 3 | |||
| rs111033690 | 0.882 | 0.120 | 9 | 34647858 | missense variant | C/G;T | snv | 4.0E-06; 2.5E-04 | 3 | ||
| rs111033773 | 0.882 | 0.200 | 9 | 34649032 | missense variant | G/T | snv | 1.4E-04 | 1.7E-04 | 3 | |
| rs368637540 | 0.882 | 0.120 | 1 | 23795992 | missense variant | C/G;T | snv | 1.2E-05 | 3 | ||
| rs949142013 | 0.925 | 0.120 | 6 | 32977541 | missense variant | G/A | snv | 2 | |||
| rs111033781 | 0.925 | 0.120 | 9 | 34649058 | missense variant | T/A | snv | 2 | |||
| rs111033795 | 0.925 | 0.120 | 9 | 34649463 | missense variant | G/A | snv | 1.2E-05 | 1.4E-05 | 2 |