| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11001553 | 0.925 | 0.080 | 10 | 52313141 | intron variant | C/T | snv | 0.12 | 2 | ||
| rs145640971 | 1.000 | 0.040 | 10 | 52314555 | missense variant | G/A | snv | 1.3E-04 | 1.3E-04 | 1 | |
| rs1896368 | 1.000 | 0.040 | 10 | 52309144 | intron variant | C/T | snv | 0.43 | 1 | ||
| rs149268042 | 1.000 | 0.040 | 10 | 52315038 | missense variant | G/T | snv | 2.9E-03 | 2.6E-03 | 1 | |
| rs10824310 | 1.000 | 0.080 | 10 | 52268704 | intron variant | C/T | snv | 4.7E-02 | 1 |