| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs80356682 | 0.790 | 0.120 | 1 | 209625721 | stop gained | G/A | snv | 5.1E-04 | 4.8E-04 | 7 | |
| rs121912771 | 0.882 | 0.080 | 10 | 104034193 | missense variant | C/T | snv | 1.1E-04 | 1.5E-04 | 3 | |
| rs121912773 | 0.925 | 0.080 | 10 | 104053072 | missense variant | C/T | snv | 2 | |||
| rs121912774 | 0.925 | 0.080 | 10 | 104072062 | stop gained | G/A | snv | 4.0E-06 | 2 | ||
| rs1181742615 | 0.925 | 0.080 | 18 | 23915298 | stop gained | C/G;T | snv | 4.0E-06; 8.0E-06 | 2 | ||
| rs121912482 | 0.925 | 0.080 | 1 | 209633070 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
| rs1210666598 | 1.000 | 0.080 | 10 | 104034272 | frameshift variant | CAGGGGGTC/C;G | delins | 4.6E-06 | 1 | ||
| rs998162536 | 1.000 | 0.080 | 18 | 23928631 | stop gained | C/G;T | snv | 4.0E-06 | 1 | ||
| rs1168634503 | 1.000 | 0.080 | 1 | 183186431 | missense variant | G/A | snv | 1 |