| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4647924 | 0.600 | 0.520 | 4 | 1801844 | missense variant | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 30 | ||
| rs45546039 | 0.732 | 0.120 | 3 | 38613781 | missense variant | C/A;T | snv | 4.1E-06 | 10 | ||
| rs199473097 | 0.763 | 0.120 | 3 | 38606710 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 9 | |
| rs757532106 | 0.763 | 0.120 | 3 | 38550500 | stop gained | G/A | snv | 4.5E-05 | 4.9E-05 | 9 | |
| rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 8 | |
| rs794728708 | 0.827 | 0.120 | 1 | 237377386 | missense variant | G/A;T | snv | 3 | |||
| rs7626962 | 0.790 | 0.080 | 3 | 38579416 | missense variant | G/A;T | snv | 1.6E-05; 5.9E-03 | 3 | ||
| rs72546668 | 0.807 | 0.200 | 3 | 8745644 | missense variant | C/A;T | snv | 4.0E-06; 2.6E-03 | 3 | ||
| rs121909281 | 0.925 | 0.120 | 3 | 8733916 | missense variant | G/A;C | snv | 4.3E-04 | 2 | ||
| rs80356779 | 0.776 | 0.320 | 11 | 68780662 | missense variant | G/A | snv | 3.2E-05 | 5.6E-05 | 2 | |
| rs199472728 | 0.925 | 0.120 | 11 | 2572885 | missense variant | A/G | snv | 1.8E-04 | 1.3E-04 | 2 | |
| rs137854609 | 0.882 | 0.120 | 3 | 38581170 | missense variant | C/A;T | snv | 7.9E-05 | 2 | ||
| rs199473124 | 0.851 | 0.120 | 3 | 38603902 | missense variant | A/T | snv | 8.0E-06 | 7.0E-06 | 2 | |
| rs199473573 | 0.925 | 0.120 | 3 | 38604007 | missense variant | A/C | snv | 1.6E-05 | 7.0E-06 | 2 | |
| rs199473604 | 0.882 | 0.120 | 3 | 38560394 | missense variant | G/T | snv | 2 | |||
| rs121909282 | 0.925 | 0.120 | 3 | 8745647 | missense variant | T/G | snv | 1.4E-05 | 2 | ||
| rs121434278 | 0.882 | 0.120 | 1 | 75740094 | missense variant | G/A | snv | 4.0E-05 | 7.0E-05 | 1 | |
| rs77931234 | 0.925 | 0.120 | 1 | 75761161 | missense variant | A/C;G | snv | 3.3E-03 | 1 | ||
| rs72552293 | 0.925 | 0.120 | 3 | 32140231 | missense variant | A/G | snv | 2.5E-03 | 2.9E-03 | 1 | |
| rs72466451 | 0.925 | 0.160 | 2 | 197498763 | missense variant | T/C | snv | 1 | |||
| rs786205867 | 0.882 | 0.080 | 1 | 111787039 | missense variant | C/T | snv | 1 | |||
| rs1805123 | 0.724 | 0.280 | 7 | 150948446 | missense variant | T/A;C;G | snv | 1.3E-05; 0.18; 8.4E-06 | 1 | ||
| rs12133079 | 1.000 | 0.040 | 1 | 160046674 | intron variant | C/A | snv | 0.13 | 1 | ||
| rs147316959 | 1.000 | 0.040 | 12 | 21765962 | missense variant | C/T | snv | 9.9E-05 | 3.1E-04 | 1 | |
| rs10494366 | 0.851 | 0.200 | 1 | 162115895 | intron variant | G/T | snv | 0.54 | 1 |