| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909573 | 1.000 | 0.080 | 1 | 173914582 | missense variant | A/G | snv | 1 | |||
| rs1411331203 | 1.000 | 0.080 | 1 | 173914564 | missense variant | G/T | snv | 7.0E-06 | 1 | ||
| rs1423630663 | 1.000 | 0.080 | 1 | 173910764 | missense variant | A/G | snv | 1 | |||
| rs1425532034 | 1.000 | 0.080 | 1 | 173911830 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs147266200 | 1.000 | 0.080 | 1 | 173914696 | missense variant | G/A | snv | 8.0E-06 | 1 | ||
| rs2227624 | 1.000 | 0.080 | 1 | 173914872 | missense variant | A/T | snv | 1.8E-03 | 1.7E-03 | 1 | |
| rs28929469 | 1.000 | 0.080 | 1 | 173914795 | missense variant | G/A | snv | 2.0E-05 | 7.0E-06 | 1 | |
| rs387906575 | 1.000 | 0.080 | 1 | 173914893 | missense variant | A/G | snv | 1 | |||
| rs483352854 | 1.000 | 0.080 | 1 | 173910875 | missense variant | G/T | snv | 1 | |||
| rs542881762 | 1.000 | 0.080 | 1 | 173907528 | intron variant | C/G;T | snv | 2.8E-05 | 1 | ||
| rs758087836 | 1.000 | 0.080 | 1 | 173909900 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs765445413 | 1.000 | 0.080 | 1 | 173911974 | missense variant | T/G | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs786204063 | 1.000 | 0.080 | 1 | 173911959 | inframe deletion | AAG/- | delins | 1 | |||
| rs863224495 | 1.000 | 0.080 | 1 | 173909645 | frameshift variant | G/- | delins | 1 | |||
| rs907768931 | 1.000 | 0.080 | 1 | 173914677 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs1188571702 | 1.000 | 0.080 | 1 | 173903962 | missense variant | A/G | snv | 1 | |||
| rs121909546 | 1.000 | 0.080 | 1 | 173903978 | missense variant | C/T | snv | 1 | |||
| rs121909548 | 1.000 | 0.080 | 1 | 173904038 | missense variant | C/A;G | snv | 8.9E-04 | 1 | ||
| rs121909554 | 1.000 | 0.080 | 1 | 173904011 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs121909566 | 1.000 | 0.080 | 1 | 173904013 | missense variant | C/T | snv | 1 | |||
| rs121909568 | 1.000 | 0.080 | 1 | 173904028 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs121909549 | 1.000 | 0.080 | 1 | 173904010 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
| rs121909550 | 1.000 | 0.080 | 1 | 173904007 | missense variant | G/A;C | snv | 1 | |||
| rs121909555 | 1.000 | 0.080 | 1 | 173903968 | missense variant | G/A | snv | 1 | |||
| rs121909557 | 1.000 | 0.080 | 1 | 173904044 | missense variant | C/T | snv | 1 |