| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
| rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
| rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 144 | ||
| rs13281615 | 0.716 | 0.360 | 8 | 127343372 | intron variant | A/G | snv | 0.43 | 18 | ||
| rs121913224 | 0.742 | 0.200 | 5 | 112839515 | frameshift variant | AAAGA/- | delins | 14 | |||
| rs1284806277 | 0.827 | 0.200 | 14 | 102251978 | missense variant | A/G | snv | 1.4E-05 | 13 | ||
| rs72550822 | 0.925 | 0.080 | 4 | 54727265 | missense variant | G/A | snv | 5.5E-04 | 1.2E-03 | 3 | |
| rs1553413200 | 1.000 | 0.080 | 2 | 47799788 | frameshift variant | -/A | delins | 1 | |||
| rs1318084062 | 1.000 | 0.080 | 11 | 111742586 | missense variant | A/G | snv | 8.0E-06 | 1 | ||
| rs121908688 | 1.000 | 0.080 | 1 | 46250097 | missense variant | C/A | snv | 1.2E-05 | 1 |