| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | ||
| rs72696020 | 1.000 | 0.080 | 14 | 88105563 | intergenic variant | G/A | snv | 9.9E-03 | 1 | ||
| rs2025009 | 1.000 | 0.080 | 14 | 68376888 | intron variant | G/A;C | snv | 1 | |||
| rs28521457 | 1.000 | 0.080 | 4 | 150759175 | intron variant | G/A;C | snv | 1 | |||
| rs114577328 | 1.000 | 0.080 | 6 | 29959505 | downstream gene variant | G/C | snv | 1.3E-02 | 2 | ||
| rs597480 | 1.000 | 0.080 | 11 | 85725825 | missense variant | G/C;T | snv | 0.59; 3.2E-05 | 1 | ||
| rs3129900 | 0.882 | 0.200 | 6 | 32338202 | intron variant | G/T | snv | 0.83 | 3 | ||
| rs116606120 | 1.000 | 0.080 | 5 | 28665845 | intron variant | T/A | snv | 1.0E-02 | 1 | ||
| rs6139258 | 1.000 | 0.080 | 20 | 3977969 | intron variant | T/C | snv | 3.2E-02 | 2 | ||
| rs114811931 | 1.000 | 0.080 | 5 | 161257724 | intergenic variant | T/C | snv | 1.8E-02 | 1 | ||
| rs7828135 | 1.000 | 0.080 | 8 | 80146584 | intron variant | T/C | snv | 0.12 | 1 | ||
| rs2395029 | 0.790 | 0.320 | 6 | 31464003 | non coding transcript exon variant | T/G | snv | 2.7E-02 | 2.4E-02 | 12 |