| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1564354968 | 0.882 | 0.040 | 10 | 13109279 | frameshift variant | -/AGCT | delins | 3 | |||
| rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
| rs751497460 | 1.000 | 0.040 | 1 | 160681173 | frameshift variant | -/T | ins | 5.6E-05 | 1 | ||
| rs547984 | 0.882 | 0.040 | 1 | 237933586 | intergenic variant | A/C | snv | 0.60 | 3 | ||
| rs11241095 | 0.925 | 0.040 | 5 | 111103810 | missense variant | A/C;G | snv | 0.33 | 3 | ||
| rs576499843 | 0.882 | 0.040 | 1 | 107617607 | missense variant | A/C;G | snv | 8.0E-06 | 7.0E-06 | 3 | |
| rs74315331 | 0.882 | 0.040 | 1 | 171636010 | missense variant | A/C;T | snv | 3 | |||
| rs7098387 | 1.000 | 0.040 | 10 | 20334544 | regulatory region variant | A/C;T | snv | 0.13 | 1 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 188 | |
| rs4880 | 0.500 | 0.840 | 6 | 159692840 | missense variant | A/G | snv | 0.48 | 0.47 | 131 | |
| rs17576 | 0.557 | 0.760 | 20 | 46011586 | missense variant | A/G | snv | 0.39 | 0.36 | 73 | |
| rs1927911 | 0.658 | 0.640 | 9 | 117707776 | intron variant | A/G | snv | 0.62 | 28 | ||
| rs523096 | 0.827 | 0.080 | 9 | 22019130 | intron variant | A/G | snv | 0.30 | 7 | ||
| rs7049105 | 0.807 | 0.120 | 9 | 22028802 | intron variant | A/G | snv | 0.58 | 7 | ||
| rs74315328 | 0.807 | 0.120 | 1 | 171636131 | missense variant | A/G | snv | 6 | |||
| rs754203 | 0.807 | 0.200 | 14 | 99691630 | non coding transcript exon variant | A/G | snv | 0.27 | 6 | ||
| rs267606929 | 0.827 | 0.120 | 10 | 13132098 | missense variant | A/G | snv | 5 | |||
| rs11669977 | 0.882 | 0.040 | 19 | 49060867 | non coding transcript exon variant | A/G | snv | 0.17 | 3 | ||
| rs3858145 | 0.882 | 0.040 | 10 | 68252081 | regulatory region variant | A/G | snv | 0.33 | 3 | ||
| rs7037117 | 0.882 | 0.040 | 9 | 117721385 | 3 prime UTR variant | A/G | snv | 0.40 | 3 | ||
| rs74315338 | 0.882 | 0.040 | 1 | 171636143 | missense variant | A/G | snv | 3 | |||
| rs34595252 | 0.925 | 0.040 | 5 | 111119021 | missense variant | A/G | snv | 4.3E-03 | 4.5E-03 | 2 | |
| rs751417985 | 0.925 | 0.040 | 11 | 64203143 | missense variant | A/G | snv | 2.4E-05 | 3.5E-05 | 2 | |
| rs755246983 | 0.925 | 0.040 | 1 | 171652539 | missense variant | A/G | snv | 8.0E-06; 4.0E-06 | 2 |