| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs118204096 | 1.000 | 0.160 | 11 | 119091432 | missense variant | G/A | snv | 3 | |||
| rs1208917022 | 1.000 | 0.040 | 12 | 6936663 | missense variant | A/G | snv | 3 | |||
| rs121918518 | 1.000 | 0.080 | 19 | 53889655 | missense variant | C/G | snv | 3 | |||
| rs1320457487 | 1.000 | 0.120 | 2 | 44301057 | missense variant | G/A | snv | 8.0E-06 | 3 | ||
| rs1424215334 | 1.000 | 0.120 | 2 | 44280805 | missense variant | A/G | snv | 2.1E-05 | 3 | ||
| rs200248046 | 1.000 | 0.120 | 2 | 44299998 | missense variant | G/A;C | snv | 4.0E-06; 8.0E-06 | 3 | ||
| rs267607044 | 1.000 | 0.080 | 9 | 132327718 | missense variant | G/A | snv | 8.0E-06 | 2.1E-05 | 3 | |
| rs587777004 | 1.000 | 0.080 | 1 | 244842055 | missense variant | A/C;G | snv | 4.0E-06 | 3 | ||
| rs1318256630 | 11 | 66708251 | missense variant | G/A | snv | 4.1E-06 | 2 | ||||
| rs876661219 | 1.000 | 12 | 13571891 | missense variant | A/C;G | snv | 2 | ||||
| rs797046006 | 11 | 66715958 | missense variant | T/C | snv | 1 | |||||
| rs3512 | 0.925 | 0.160 | 15 | 30942802 | 3 prime UTR variant | G/C | snv | 0.27 | 4 | ||
| rs1135401778 | 0.752 | 0.400 | 17 | 67854315 | frameshift variant | T/- | del | 20 | |||
| rs1553281318 | 0.882 | 0.120 | 1 | 226986536 | frameshift variant | -/A | delins | 7 | |||
| rs730882198 | 0.851 | 0.200 | 13 | 36314259 | frameshift variant | -/T | delins | 1.2E-05 | 6 | ||
| rs730882209 | 0.925 | 0.080 | 9 | 132326375 | frameshift variant | -/C | delins | 6 | |||
| rs1553878395 | 0.925 | 0.080 | 4 | 25127263 | splice acceptor variant | AAAGATATGGGATTGTGAGGTGTATGCAACAGTCTTTCATTGTAGGCTTCTGACAACTTCTTTATTTGGTTGGACAAATATGAAAACATTTCCT/- | delins | 5 | |||
| rs181109321 | 0.776 | 0.320 | 8 | 63065904 | splice region variant | C/A;T | snv | 2.0E-05 | 17 |