| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7531806 | 1.000 | 0.040 | 1 | 169681903 | intron variant | G/A | snv | 0.61 | 1 | ||
| rs2242095 | 1.000 | 0.040 | 8 | 143596704 | 5 prime UTR variant | C/T | snv | 0.15 | 1 | ||
| rs28570522 | 1.000 | 0.040 | 8 | 10773058 | intron variant | A/G | snv | 0.66 | 1 | ||
| rs158639 | 1.000 | 0.040 | 5 | 56315883 | intron variant | G/A | snv | 0.33 | 1 | ||
| rs11118336 | 1.000 | 0.040 | 1 | 219547941 | intergenic variant | C/T | snv | 0.51 | 1 | ||
| rs1256580 | 1.000 | 0.040 | 1 | 219026038 | intron variant | G/C | snv | 0.29 | 1 | ||
| rs144991069 | 1.000 | 0.040 | 11 | 65060236 | upstream gene variant | T/A | snv | 6.8E-03 | 1 | ||
| rs61744384 | 1.000 | 0.040 | 11 | 65619907 | synonymous variant | T/A;G | snv | 0.45; 4.1E-06 | 1 | ||
| rs1533326 | 1.000 | 0.040 | 15 | 90211722 | intron variant | A/G | snv | 0.39 | 1 | ||
| rs7809981 | 1.000 | 0.040 | 7 | 40834777 | intron variant | G/T | snv | 0.24 | 1 | ||
| rs28405582 | 1.000 | 0.040 | 3 | 23863271 | intron variant | T/C | snv | 4.6E-02 | 1 | ||
| rs72966077 | 1.000 | 0.040 | 2 | 218894507 | intron variant | C/T | snv | 3.3E-02 | 1 |