| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913355 | 0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 | 4 | ||
| rs121913499 | 0.605 | 0.520 | 2 | 208248389 | missense variant | G/A;C;T | snv | 2 | |||
| rs121913338 | 0.677 | 0.400 | 7 | 140753354 | missense variant | T/A;C;G | snv | 1 | |||
| rs121913357 | 0.742 | 0.320 | 7 | 140781603 | stop gained | C/A;G;T | snv | 1 | |||
| rs777919630 | 0.623 | 0.680 | 21 | 43062358 | missense variant | G/A;T | snv | 8.0E-06; 4.0E-06 | 1 | ||
| rs606231364 | 0.925 | 0.160 | 10 | 89003071 | missense variant | G/A | snv | 1 | |||
| rs758835365 | 1.000 | 0.120 | 10 | 89010795 | stop gained | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs351855 | 0.597 | 0.560 | 5 | 177093242 | missense variant | G/A | snv | 0.33 | 0.26 | 1 | |
| rs2236225 | 0.614 | 0.640 | 14 | 64442127 | missense variant | G/A | snv | 0.44 | 0.38 | 1 | |
| rs114216685 | 1.000 | 0.120 | 8 | 94391640 | missense variant | T/C | snv | 8.8E-04 | 3.9E-04 | 1 | |
| rs121908689 | 0.925 | 0.120 | 1 | 46272758 | missense variant | T/A | snv | 1 |