| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
| rs199473190 | 1.000 | 0.040 | 3 | 38579474 | missense variant | C/G;T | snv | 8.2E-06 | 1 | ||
| rs199473097 | 0.763 | 0.120 | 3 | 38606710 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 9 | |
| rs199473124 | 0.851 | 0.120 | 3 | 38603902 | missense variant | A/T | snv | 8.0E-06 | 7.0E-06 | 4 | |
| rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
| rs1188884950 | 0.925 | 0.080 | 5 | 474952 | missense variant | A/G | snv | 4.2E-06 | 2 | ||
| rs4647924 | 0.600 | 0.520 | 4 | 1801844 | missense variant | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 49 | ||
| rs45546039 | 0.732 | 0.120 | 3 | 38613781 | missense variant | C/A;T | snv | 4.1E-06 | 15 | ||
| rs1310230286 | 1.000 | 0.040 | 3 | 38604872 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs751377893 | 0.574 | 0.680 | 1 | 169546513 | missense variant | T/C | snv | 4.0E-06 | 65 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs899127658 | 0.547 | 0.720 | 11 | 46739084 | missense variant | G/A;C | snv | 82 | |||
| rs25531 | 0.581 | 0.520 | 17 | 30237328 | upstream gene variant | T/C | snv | 0.18 | 72 | ||
| rs2069705 | 0.695 | 0.440 | 12 | 68161231 | intron variant | G/A;C | snv | 19 | |||
| rs767910122 | 0.724 | 0.280 | 7 | 150948446 | frameshift variant | -/GTCCG | ins | 4.4E-05 | 17 | ||
| rs794728448 | 0.724 | 0.280 | 7 | 150948445 | frameshift variant | CT/G | delins | 17 | |||
| rs2069718 | 0.742 | 0.320 | 12 | 68156382 | intron variant | A/G;T | snv | 0.50 | 14 | ||
| rs1318358361 | 0.724 | 0.240 | 6 | 156778678 | missense variant | C/G | snv | 2.1E-05 | 13 | ||
| rs2069727 | 0.763 | 0.320 | 12 | 68154443 | intron variant | T/A;C | snv | 9 | |||
| rs794728708 | 0.827 | 0.120 | 1 | 237377386 | missense variant | G/A;T | snv | 8 | |||
| rs10494366 | 0.851 | 0.200 | 1 | 162115895 | intron variant | G/T | snv | 0.54 | 7 | ||
| rs2075575 | 0.851 | 0.200 | 18 | 26866562 | intron variant | G/A | snv | 0.31 | 5 | ||
| rs9951307 | 0.882 | 0.120 | 18 | 26850565 | intron variant | G/A | snv | 0.65 | 5 | ||
| rs199473604 | 0.882 | 0.120 | 3 | 38560394 | missense variant | G/T | snv | 4 | |||
| rs786205867 | 0.882 | 0.080 | 1 | 111787039 | missense variant | C/T | snv | 3 |