| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs186920977 | 1.000 | 0.080 | 2 | 56422795 | intergenic variant | G/A | snv | 1.1E-02 | 1 | ||
| rs191153876 | 1.000 | 0.080 | 3 | 123918335 | intron variant | A/T | snv | 1.4E-02 | 1 | ||
| rs2025009 | 1.000 | 0.080 | 14 | 68376888 | intron variant | G/A;C | snv | 1 | |||
| rs2240395 | 1.000 | 0.080 | 7 | 140018347 | intron variant | C/G;T | snv | 0.41 | 1 | ||
| rs2523822 | 1.000 | 0.080 | 6 | 29860883 | intron variant | A/G | snv | 0.26 | 1 | ||
| rs28521457 | 1.000 | 0.080 | 4 | 150759175 | intron variant | G/A;C | snv | 1 | |||
| rs597480 | 1.000 | 0.080 | 11 | 85725825 | missense variant | G/C;T | snv | 0.59; 3.2E-05 | 1 | ||
| rs61858823 | 1.000 | 0.080 | 10 | 65095495 | intergenic variant | G/A | snv | 1.3E-02 | 1 | ||
| rs6582630 | 1.000 | 0.080 | 12 | 38349706 | intergenic variant | G/A | snv | 0.62 | 1 | ||
| rs6694270 | 1.000 | 0.080 | 1 | 18793883 | intergenic variant | A/G | snv | 0.26 | 1 | ||
| rs72696020 | 1.000 | 0.080 | 14 | 88105563 | intergenic variant | G/A | snv | 9.9E-03 | 1 | ||
| rs73122578 | 1.000 | 0.080 | 3 | 79310483 | intron variant | A/C | snv | 0.27 | 1 | ||
| rs7828135 | 1.000 | 0.080 | 8 | 80146584 | intron variant | T/C | snv | 0.12 | 1 |