| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10490924 | 0.716 | 0.240 | 10 | 122454932 | missense variant | G/T | snv | 0.26 | 0.23 | 16 | |
| rs3750846 | 0.851 | 0.040 | 10 | 122456049 | intron variant | T/C | snv | 0.24 | 4 | ||
| rs3750847 | 0.882 | 0.040 | 10 | 122455905 | intron variant | C/T | snv | 0.23 | 4 | ||
| rs2736911 | 0.882 | 0.120 | 10 | 122454839 | stop gained | C/A;T | snv | 4.0E-06; 0.13 | 3 | ||
| rs10490923 | 0.925 | 0.160 | 10 | 122454735 | missense variant | G/A | snv | 0.11 | 9.2E-02 | 2 | |
| rs10664316 | 1.000 | 10 | 122456869 | intron variant | -/A;AC | ins | 7.7E-05 | 1 | |||
| rs36212732 | 1.000 | 0.040 | 10 | 122455682 | intron variant | A/G | snv | 0.23 | 1 | ||
| rs36212733 | 1.000 | 0.040 | 10 | 122455695 | intron variant | T/C | snv | 0.23 | 1 | ||
| rs3750848 | 1.000 | 0.040 | 10 | 122455799 | intron variant | T/G | snv | 0.23 | 1 |