| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909637 | 0.882 | 0.240 | 8 | 38418249 | missense variant | C/A;T | snv | 1.2E-05; 2.0E-05 | 3 | ||
| rs761885185 | 0.882 | 0.120 | 3 | 189869329 | missense variant | C/T | snv | 4.0E-06 | 3 | ||
| rs121918349 | 0.925 | 0.120 | 12 | 48966271 | missense variant | G/A;C;T | snv | 8.0E-06; 4.0E-06; 4.0E-06 | 2 | ||
| rs1370886145 | 1.000 | 0.040 | 10 | 101770403 | missense variant | C/T | snv | 1.3E-05 | 1 | ||
| rs141402957 | 1.000 | 0.040 | 17 | 7670658 | missense variant | T/C | snv | 1 | |||
| rs34201045 | 1.000 | 0.040 | 3 | 189789729 | 5 prime UTR variant | -/AG;AGA;AGAG;AGG;AGGG | ins | 1 |