| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1554263366 | 1.000 | 0.040 | 6 | 145686284 | missense variant | T/C | snv | 1 | |||
| rs1554626549 | 1.000 | 0.040 | 8 | 132170427 | missense variant | G/A | snv | 1 | |||
| rs1554759745 | 1.000 | 0.040 | 9 | 128611792 | missense variant | G/A | snv | 1 | |||
| rs1554770659 | 1.000 | 0.040 | 9 | 137163819 | missense variant | T/C | snv | 1 | |||
| rs1555437424 | 1.000 | 0.040 | 15 | 92924407 | missense variant | G/A | snv | 1 | |||
| rs1555445693 | 1.000 | 0.040 | 15 | 93014832 | missense variant | C/T | snv | 1 | |||
| rs1555482933 | 0.925 | 0.040 | 16 | 9764834 | missense variant | T/A | snv | 2 | |||
| rs1555488144 | 0.925 | 0.040 | 16 | 9798454 | missense variant | C/T | snv | 2 | |||
| rs1555491648 | 0.925 | 0.040 | 16 | 9822337 | missense variant | G/A | snv | 2 | |||
| rs1555494676 | 1.000 | 0.040 | 16 | 9840657 | inframe deletion | AAG/- | delins | 1 | |||
| rs1555496111 | 0.925 | 0.040 | 16 | 9849778 | missense variant | A/G | snv | 2 | |||
| rs1555699052 | 1.000 | 0.040 | 17 | 63710782 | missense variant | C/T | snv | 1 | |||
| rs1555790846 | 1.000 | 0.040 | 20 | 8790220 | missense variant | C/T | snv | 1 | |||
| rs1555841977 | 1.000 | 0.040 | 21 | 6116503 | missense variant | C/T | snv | 1 | |||
| rs1555897392 | 1.000 | 0.040 | 22 | 31838822 | protein altering variant | -/AGA | ins | 1 | |||
| rs180922748 | 1.000 | 0.040 | 2 | 166233432 | missense variant | G/C | snv | 1.2E-03 | 1.7E-03 | 1 | |
| rs187334123 | 1.000 | 0.040 | 22 | 31797646 | missense variant | G/A;T | snv | 2.2E-03; 1.6E-05 | 1 | ||
| rs191333060 | 1.000 | 0.040 | X | 100296405 | missense variant | G/A;C | snv | 1.3E-03 | 1 | ||
| rs199692186 | 1.000 | 0.040 | 2 | 166272748 | missense variant | T/C | snv | 6.3E-04 | 5.5E-04 | 1 | |
| rs200124755 | 1.000 | 0.040 | 7 | 103498074 | splice region variant | T/G | snv | 5.2E-04 | 2.9E-04 | 1 | |
| rs200138205 | 1.000 | 0.040 | 2 | 165365200 | missense variant | G/A;C | snv | 1.7E-04; 3.2E-05 | 1 | ||
| rs201868078 | 0.925 | 0.040 | 20 | 63408524 | missense variant | G/A;C | snv | 1.6E-05 | 2 | ||
| rs202020647 | 1.000 | 0.040 | 1 | 37540752 | missense variant | G/A | snv | 1.8E-04 | 1.3E-04 | 1 | |
| rs202162520 | 1.000 | 0.040 | 16 | 2496317 | missense variant | C/A;T | snv | 4.0E-06; 1.9E-03 | 1 | ||
| rs202170644 | 1.000 | 0.040 | 3 | 64147176 | missense variant | C/G | snv | 4.7E-04 | 6.3E-04 | 1 |