| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894230 | 0.564 | 0.600 | 11 | 534288 | missense variant | C/A;G;T | snv | 73 | |||
| rs28933979 | 0.587 | 0.600 | 18 | 31592974 | missense variant | G/A;C | snv | 1.0E-04 | 70 | ||
| rs104894228 | 0.605 | 0.560 | 11 | 534286 | missense variant | C/A;G;T | snv | 48 | |||
| rs1805123 | 0.724 | 0.280 | 7 | 150948446 | missense variant | T/A;C;G | snv | 1.3E-05; 0.18; 8.4E-06 | 18 | ||
| rs143624519 | 0.724 | 0.240 | 17 | 45991484 | missense variant | G/A;T | snv | 1.5E-03; 1.2E-05 | 17 | ||
| rs794728448 | 0.724 | 0.280 | 7 | 150948445 | frameshift variant | CT/G | delins | 17 | |||
| rs137854618 | 0.742 | 0.120 | 3 | 38566426 | missense variant | C/A;T | snv | 8.0E-06 | 15 | ||
| rs120074192 | 0.763 | 0.120 | 11 | 2527959 | missense variant | A/G | snv | 10 | |||
| rs1805128 | 0.776 | 0.160 | 21 | 34449382 | missense variant | C/T | snv | 9.4E-03 | 10 | ||
| rs7626962 | 0.790 | 0.080 | 3 | 38579416 | missense variant | G/A;T | snv | 1.6E-05; 5.9E-03 | 10 | ||
| rs80338777 | 0.827 | 0.200 | 1 | 201077915 | missense variant | C/A;T | snv | 1.2E-05 | 10 | ||
| rs3766871 | 0.790 | 0.240 | 1 | 237614784 | missense variant | G/A;T | snv | 4.0E-02 | 9 | ||
| rs794728708 | 0.827 | 0.120 | 1 | 237377386 | missense variant | G/A;T | snv | 8 | |||
| rs199473605 | 0.851 | 0.120 | 3 | 38560374 | missense variant | C/G;T | snv | 4.8E-05; 4.0E-06 | 7 | ||
| rs199473225 | 0.851 | 0.120 | 3 | 38560397 | missense variant | G/A;C | snv | 6 | |||
| rs104894021 | 0.851 | 0.120 | 7 | 150951629 | missense variant | G/C;T | snv | 5 | |||
| rs104894584 | 0.851 | 0.120 | 17 | 70175553 | missense variant | G/A | snv | 5 | |||
| rs199472936 | 0.882 | 0.120 | 7 | 150951592 | missense variant | C/A;T | snv | 5 | |||
| rs374528680 | 0.851 | 0.240 | 12 | 2686216 | missense variant | G/A;C | snv | 4.0E-06; 6.0E-05 | 5 | ||
| rs869025337 | 0.925 | 0.120 | 6 | 105124593 | missense variant | G/A;C | snv | 4.0E-06 | 5 | ||
| rs121912507 | 0.882 | 0.120 | 7 | 150951511 | missense variant | C/G;T | snv | 4 | |||
| rs137854606 | 0.882 | 0.120 | 3 | 38604062 | missense variant | C/A | snv | 4 | |||
| rs1800172 | 0.925 | 0.120 | 11 | 2847899 | missense variant | G/A;T | snv | 6.2E-03 | 4 | ||
| rs199472708 | 0.882 | 0.080 | 11 | 2572015 | missense variant | G/A | snv | 4 | |||
| rs199473401 | 0.925 | 0.120 | 11 | 2570722 | missense variant | T/C | snv | 4 |