| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs76763715 | 0.658 | 0.520 | 1 | 155235843 | missense variant | T/C;G | snv | 2.3E-03 | 35 | ||
| rs1064651 | 0.732 | 0.360 | 1 | 155235727 | missense variant | C/G | snv | 1.3E-04 | 2.0E-04 | 13 | |
| rs75822236 | 0.752 | 0.200 | 1 | 155235002 | missense variant | C/T | snv | 1.8E-04 | 6.1E-05 | 10 | |
| rs80356772 | 0.790 | 0.160 | 1 | 155235195 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 9 | |
| rs104886460 | 0.776 | 0.160 | 1 | 155240629 | splice donor variant | C/A;T | snv | 7.6E-05 | 8 | ||
| rs78973108 | 0.776 | 0.160 | 1 | 155237453 | missense variant | C/T | snv | 2.8E-05 | 4.2E-05 | 8 | |
| rs80356769 | 0.776 | 0.160 | 1 | 155235772 | missense variant | C/A | snv | 3.2E-05 | 7.0E-06 | 8 | |
| rs80356771 | 0.776 | 0.160 | 1 | 155235196 | missense variant | G/A;T | snv | 7.2E-05; 4.0E-06 | 8 | ||
| rs1064644 | 0.807 | 0.120 | 1 | 155238192 | missense variant | A/G | snv | 8.0E-06 | 6 | ||
| rs79653797 | 0.851 | 0.120 | 1 | 155238629 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 4 | ||
| rs80356763 | 0.882 | 0.120 | 1 | 155238596 | missense variant | C/A;T | snv | 4.0E-06; 2.4E-05 | 3 | ||
| rs80356768 | 0.882 | 0.120 | 1 | 155235750 | frameshift variant | ACTGTCGACAAAGTTACGCACCCAATTGGGTCCTCCTTCGGGGTTCAGGGCAAGG/- | delins | 3 | |||
| rs121908309 | 0.925 | 0.120 | 1 | 155236277 | stop gained | G/A | snv | 4.0E-06 | 2 | ||
| rs121908310 | 0.925 | 0.120 | 1 | 155235760 | missense variant | C/A;G | snv | 4.0E-06 | 2 | ||
| rs121908313 | 0.925 | 0.120 | 1 | 155237470 | missense variant | G/T | snv | 2 | |||
| rs74462743 | 0.925 | 0.120 | 1 | 155238194 | missense variant | C/T | snv | 8.0E-06 | 2 | ||
| rs397518434 | 1.000 | 0.120 | 1 | 155238572 | frameshift variant | G/- | delins | 1 | |||
| rs78198234 | 1.000 | 0.120 | 1 | 155236420 | missense variant | T/A;C | snv | 4.0E-06 | 1 |