| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2855812 | 0.790 | 0.360 | 6 | 31504943 | intron variant | G/T | snv | 0.23 | 6 | ||
| rs10947233 | 0.925 | 0.160 | 6 | 32156647 | intron variant | G/C;T | snv | 3.4E-02 | 4 | ||
| rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 4 | |
| rs2856437 | 1.000 | 0.120 | 6 | 32189587 | intron variant | G/A | snv | 3.7E-02 | 3 | ||
| rs8192575 | 1.000 | 0.120 | 6 | 32198607 | intron variant | C/G;T | snv | 7.0E-02; 4.1E-06 | 3 |