| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs727505376 | 0.925 | 0.160 | 8 | 38414279 | missense variant | C/G;T | snv | 2 | |||
| rs781328162 | 0.925 | 0.160 | 8 | 38413714 | missense variant | C/T | snv | 2.0E-05 | 3.5E-05 | 2 | |
| rs104893842 | 0.925 | 0.040 | 4 | 67753920 | missense variant | C/T | snv | 1.4E-04 | 2.1E-04 | 2 | |
| rs199538589 | 0.925 | 0.040 | 2 | 128268254 | missense variant | G/A | snv | 1.9E-03 | 9.3E-04 | 2 | |
| rs104894701 | 0.925 | 0.040 | 19 | 920542 | stop gained | C/T | snv | 7.0E-06 | 2 | ||
| rs104894702 | 0.925 | 0.040 | 19 | 920746 | stop lost | T/A;C | snv | 6.8E-05 | 2 | ||
| rs606231407 | 1.000 | 0.040 | 10 | 101770613 | missense variant | C/T | snv | 1.6E-05 | 2 | ||
| rs121918340 | 0.925 | 0.040 | 9 | 137449656 | missense variant | T/C | snv | 2 | |||
| rs376239580 | 0.925 | 0.040 | 20 | 5302632 | missense variant | G/A | snv | 1.2E-05 | 2.1E-05 | 2 | |
| rs730882248 | 0.925 | 0.160 | 7 | 5711761 | splice region variant | C/T | snv | 2 | |||
| rs104893843 | 0.925 | 0.040 | 4 | 67754306 | missense variant | A/T | snv | 1.3E-04 | 6.3E-05 | 2 | |
| rs727505367 | 1.000 | 0.040 | 4 | 67753986 | missense variant | A/C | snv | 1.4E-05 | 2 | ||
| rs186630563 | 1.000 | 0.040 | X | 8699739 | missense variant | C/T | snv | 2.1E-04 | 7.2E-04 | 1 | |
| rs1224900173 | 1.000 | 0.040 | 4 | 147519933 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs1064793123 | 1.000 | 0.040 | 8 | 38421859 | missense variant | G/A | snv | 1 | |||
| rs727505377 | 1.000 | 0.040 | 8 | 38414001 | missense variant | A/G | snv | 1 | |||
| rs104893838 | 1.000 | 0.040 | 4 | 67753950 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06; 1.6E-05 | 1 | ||
| rs104893839 | 1.000 | 0.040 | 4 | 67744659 | missense variant | G/T | snv | 1 | |||
| rs104893840 | 1.000 | 0.040 | 4 | 67753832 | missense variant | A/T | snv | 1 | |||
| rs104893841 | 1.000 | 0.040 | 4 | 67740526 | stop gained | A/T | snv | 1 | |||
| rs1391808526 | 1.000 | 0.040 | 4 | 67754089 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs144900788 | 1.000 | 0.040 | 4 | 67753900 | missense variant | G/A;T | snv | 1.3E-03 | 1 | ||
| rs28933074 | 1.000 | 0.040 | 4 | 67740616 | missense variant | T/C | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs774317793 | 1.000 | 0.040 | 4 | 67754283 | missense variant | T/C | snv | 1.9E-04 | 2.1E-05 | 1 | |
| rs1445182466 | 1.000 | 0.040 | 6 | 116809366 | missense variant | G/A | snv | 1 |