| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs375045125 | 1.000 | 0.040 | 1 | 151429672 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs548226228 | 1.000 | 0.040 | 1 | 151406914 | missense variant | G/A | snv | 1.2E-05 | 2.1E-05 | 1 | |
| rs561369202 | 1.000 | 0.040 | 1 | 151428152 | missense variant | T/C | snv | 6.4E-05 | 1.4E-05 | 1 | |
| rs574158925 | 1.000 | 0.040 | 1 | 151427829 | missense variant | T/C | snv | 5.6E-05 | 2.8E-05 | 1 | |
| rs574335012 | 1.000 | 0.040 | 1 | 151427959 | missense variant | G/C | snv | 1.2E-05 | 1 | ||
| rs749270162 | 1.000 | 0.040 | 1 | 151406620 | missense variant | T/C | snv | 2.4E-05 | 1 | ||
| rs749548928 | 1.000 | 0.040 | 1 | 151408815 | missense variant | T/C;G | snv | 4.0E-06 | 1 | ||
| rs753214391 | 1.000 | 0.040 | 1 | 151406444 | missense variant | C/T | snv | 1.0E-05 | 2.1E-05 | 1 | |
| rs754532606 | 1.000 | 0.040 | 1 | 151423526 | missense variant | C/T | snv | 8.0E-06 | 2.1E-05 | 1 | |
| rs756691187 | 1.000 | 0.040 | 1 | 151404993 | missense variant | C/G | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs760059077 | 1.000 | 0.040 | 1 | 151405919 | missense variant | C/T | snv | 2.4E-05 | 2.1E-05 | 1 | |
| rs760211123 | 1.000 | 0.040 | 1 | 151405662 | missense variant | T/C | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs763820362 | 1.000 | 0.040 | 1 | 151424045 | missense variant | C/T | snv | 2.4E-05 | 1 | ||
| rs769581210 | 1.000 | 0.040 | 1 | 151405376 | missense variant | T/C | snv | 7.2E-05 | 3.5E-05 | 1 | |
| rs772572695 | 1.000 | 0.040 | 1 | 151406427 | missense variant | C/A;T | snv | 2.5E-05 | 1 | ||
| rs778792467 | 1.000 | 0.040 | 1 | 151405692 | missense variant | G/C | snv | 4.4E-05 | 7.0E-06 | 1 | |
| rs866632178 | 1.000 | 0.040 | 1 | 151441000 | missense variant | C/T | snv | 1.6E-05 | 1.4E-05 | 1 | |
| rs888864913 | 1.000 | 0.040 | 1 | 151424097 | missense variant | C/T | snv | 1.2E-05 | 2.8E-05 | 1 | |
| rs998675361 | 1.000 | 0.040 | 1 | 151430806 | missense variant | G/A;C | snv | 9.0E-06 | 1 | ||
| rs797045050 | 0.807 | 0.120 | 2 | 240797715 | missense variant | C/T | snv | 4 | |||
| rs121918799 | 0.752 | 0.120 | 2 | 166015636 | missense variant | G/C | snv | 1.7E-03 | 1.6E-03 | 2 | |
| rs1553518509 | 1.000 | 0.040 | 2 | 148468916 | stop gained | C/T | snv | 2 | |||
| rs10497655 | 1.000 | 0.040 | 2 | 184597314 | intron variant | T/C;G | snv | 1 | |||
| rs2289195 | 1.000 | 0.040 | 2 | 25240614 | intron variant | G/A | snv | 0.41 | 0.41 | 1 | |
| rs112795301 | 0.776 | 0.160 | 3 | 70972634 | stop gained | G/A | snv | 11 |