| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs185305928 | 1.000 | 0.080 | 1 | 6845651 | intron variant | G/A | snv | 9.3E-03 | 1 | ||
| rs191153876 | 1.000 | 0.080 | 3 | 123918335 | intron variant | A/T | snv | 1.4E-02 | 1 | ||
| rs115266745 | 1.000 | 0.080 | 3 | 779530 | intron variant | A/C | snv | 8.3E-03 | 1 | ||
| rs1497546 | 1.000 | 0.080 | 3 | 98315682 | intron variant | G/A | snv | 9.0E-02 | 1 | ||
| rs28521457 | 1.000 | 0.080 | 4 | 150759175 | intron variant | G/A;C | snv | 1 | |||
| rs143575776 | 1.000 | 0.080 | 9 | 9593742 | intron variant | A/T | snv | 1.2E-02 | 1 | ||
| rs112655218 | 1.000 | 0.080 | 18 | 9841518 | non coding transcript exon variant | G/A | snv | 5.0E-02 | 1 | ||
| rs2025009 | 1.000 | 0.080 | 14 | 68376888 | intron variant | G/A;C | snv | 1 | |||
| rs73122578 | 1.000 | 0.080 | 3 | 79310483 | intron variant | A/C | snv | 0.27 | 1 | ||
| rs10937275 | 1.000 | 0.080 | 3 | 186933001 | intron variant | A/G | snv | 0.88 | 1 | ||
| rs597480 | 1.000 | 0.080 | 11 | 85725825 | missense variant | G/C;T | snv | 0.59; 3.2E-05 | 1 | ||
| rs2240395 | 1.000 | 0.080 | 7 | 140018347 | intron variant | C/G;T | snv | 0.41 | 1 | ||
| rs7828135 | 1.000 | 0.080 | 8 | 80146584 | intron variant | T/C | snv | 0.12 | 1 |