| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1870377 | 0.695 | 0.520 | 4 | 55106807 | missense variant | T/A | snv | 0.22 | 0.20 | 25 | |
| rs121913409 | 0.708 | 0.400 | 3 | 41224646 | missense variant | C/A;G;T | snv | 21 | |||
| rs121913412 | 0.724 | 0.280 | 3 | 41224633 | missense variant | A/C;G;T | snv | 19 | |||
| rs3822214 | 0.732 | 0.240 | 4 | 54727298 | missense variant | A/C;G;T | snv | 7.7E-02; 8.0E-06 | 13 | ||
| rs559510809 | 0.882 | 0.120 | 5 | 112819294 | stop gained | G/A;T | snv | 4.0E-06 | 3 | ||
| rs398123122 | 0.925 | 0.120 | 5 | 112840063 | frameshift variant | -/T | delins | 2 | |||
| rs774104442 | 1.000 | 0.040 | 10 | 67607015 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs1171472831 | 1.000 | 0.040 | 3 | 41224664 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs145640971 | 1.000 | 0.040 | 10 | 52314555 | missense variant | G/A | snv | 1.3E-04 | 1.3E-04 | 1 | |
| rs1363478606 | 1.000 | 0.040 | 8 | 140890686 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs756906833 | 1.000 | 0.040 | 8 | 140890680 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs776599337 | 1.000 | 0.040 | 8 | 140744759 | frameshift variant | TG/- | del | 1 |