| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs770374710 | 0.611 | 0.560 | 15 | 23645747 | frameshift variant | G/-;GG | delins | 87 | |||
| rs1564421528 | 0.882 | 0.080 | 10 | 28614666 | stop gained | C/T | snv | 16 | |||
| rs121918654 | 0.882 | 0.200 | 9 | 124503218 | missense variant | GC/TT | mnv | 6 | |||
| rs6161 | 0.851 | 0.080 | 15 | 74343027 | missense variant | C/T | snv | 2.5E-03 | 2.6E-03 | 5 | |
| rs121918655 | 0.851 | 0.200 | 9 | 124493143 | missense variant | C/T | snv | 5 | |||
| rs104894897 | 0.882 | 0.160 | X | 30304676 | missense variant | A/C | snv | 4 | |||
| rs104894118 | 0.882 | 0.080 | 9 | 124500196 | missense variant | C/A;T | snv | 1.6E-05; 4.1E-06 | 4 | ||
| rs1284060395 | 0.925 | 0.160 | 15 | 74339666 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 3 | |
| rs1454328072 | 0.925 | 0.160 | 15 | 74339260 | stop gained | G/A | snv | 4.0E-06 | 3 | ||
| rs775130992 | 1.000 | 0.040 | 8 | 38146310 | missense variant | G/T | snv | 4.0E-06 | 3 |