| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121912426 | 1.000 | 0.080 | 15 | 98707880 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
| rs121912427 | 1.000 | 0.080 | 15 | 98707902 | missense variant | A/C;G | snv | 1.2E-05 | 1 | ||
| rs121912429 | 1.000 | 0.080 | 15 | 98922162 | missense variant | G/A | snv | 1.2E-05 | 2.1E-05 | 1 | |
| rs141802822 | 1.000 | 0.080 | 15 | 98957347 | missense variant | C/T | snv | 3.3E-04 | 6.8E-04 | 1 |