| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10131567 | 1.000 | 0.040 | 14 | 35395672 | intergenic variant | G/T | snv | 0.22 | 1 | ||
| rs10244416 | 1.000 | 0.040 | 7 | 20536128 | intergenic variant | C/A;T | snv | 0.52 | 1 | ||
| rs10468514 | 1.000 | 0.040 | 17 | 45378874 | intergenic variant | A/G | snv | 0.38 | 1 | ||
| rs10489854 | 1.000 | 0.040 | 1 | 159279069 | non coding transcript exon variant | C/T | snv | 8.3E-02 | 1 | ||
| rs111267073 | 1.000 | 0.040 | 5 | 111030094 | intergenic variant | C/T | snv | 1.9E-02 | 1 | ||
| rs11213941 | 1.000 | 0.040 | 11 | 111563369 | downstream gene variant | T/C | snv | 0.35 | 1 | ||
| rs114997373 | 1.000 | 0.040 | 1 | 45535906 | downstream gene variant | G/A | snv | 1.2E-02 | 1 | ||
| rs118013485 | 1.000 | 0.040 | 19 | 33235671 | TF binding site variant | G/A | snv | 5.0E-02 | 1 | ||
| rs12282231 | 1.000 | 0.040 | 11 | 2274398 | upstream gene variant | C/T | snv | 9.0E-02 | 1 | ||
| rs12760882 | 1.000 | 0.040 | 1 | 9285727 | intergenic variant | T/A | snv | 0.32 | 1 | ||
| rs12886625 | 1.000 | 0.040 | 14 | 102772597 | intron variant | C/G | snv | 0.38 | 1 | ||
| rs13169267 | 1.000 | 0.040 | 5 | 35573544 | intergenic variant | G/A | snv | 1.2E-02 | 1 | ||
| rs13185930 | 1.000 | 0.040 | 5 | 138241824 | intergenic variant | G/A | snv | 0.22 | 1 | ||
| rs13323006 | 1.000 | 0.040 | 3 | 112904703 | regulatory region variant | A/G | snv | 0.31 | 1 | ||
| rs1843935 | 1.000 | 0.040 | 7 | 3077159 | intergenic variant | C/A;T | snv | 0.21 | 1 | ||
| rs1905499 | 1.000 | 0.040 | 3 | 176998130 | intergenic variant | G/T | snv | 0.37 | 1 | ||
| rs2422254 | 1.000 | 0.040 | 1 | 172810693 | intron variant | T/A;C | snv | 1 | |||
| rs2511211 | 1.000 | 0.040 | 1 | 159260681 | intergenic variant | T/G | snv | 0.15 | 1 | ||
| rs2723197 | 1.000 | 0.040 | 2 | 112932170 | upstream gene variant | G/A | snv | 0.36 | 1 | ||
| rs2846072 | 1.000 | 0.040 | 11 | 76269481 | regulatory region variant | T/A;C | snv | 1 | |||
| rs28568568 | 1.000 | 0.040 | 5 | 51678216 | intergenic variant | A/T | snv | 0.26 | 1 | ||
| rs343473 | 1.000 | 0.040 | 9 | 6074936 | regulatory region variant | A/G | snv | 0.68 | 1 | ||
| rs41190 | 1.000 | 0.040 | 16 | 49245091 | intron variant | C/A | snv | 0.83 | 1 | ||
| rs56095240 | 1.000 | 0.040 | 11 | 95688666 | intron variant | T/A;C | snv | 1 | |||
| rs57453899 | 1.000 | 0.040 | 7 | 50212812 | intron variant | G/A | snv | 0.24 | 1 |