| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
| rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
| rs59616921 | 0.807 | 0.120 | 17 | 41571506 | missense variant | G/A | snv | 7 | |||
| rs149660944 | 0.851 | 0.200 | 19 | 33772017 | missense variant | C/A;T | snv | 6.5E-05; 4.0E-03 | 5 | ||
| rs199473704 | 0.882 | 0.080 | 17 | 3524224 | missense variant | C/A;T | snv | 5 | |||
| rs151339002 | 1.000 | 8 | 103329863 | stop gained | G/A;T | snv | 4.0E-06 | 2 |