| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10038271 | 1.000 | 0.040 | 5 | 157043390 | intron variant | C/T | snv | 0.16 | 1 | ||
| rs10127016 | 1.000 | 0.040 | X | 53122914 | intron variant | G/T | snv | 1 | |||
| rs11095197 | 1.000 | 0.040 | X | 30958830 | intron variant | C/T | snv | 0.28 | 1 | ||
| rs12387999 | 1.000 | 0.040 | X | 48035670 | intron variant | G/A | snv | 5.0E-02 | 1 | ||
| rs1336698 | 1.000 | 0.040 | 13 | 102211398 | intron variant | C/T | snv | 0.85 | 1 | ||
| rs16910534 | 1.000 | 0.040 | 10 | 57337568 | intergenic variant | C/T | snv | 3.1E-02 | 1 | ||
| rs17140937 | 1.000 | 0.040 | 7 | 118148430 | intergenic variant | T/C | snv | 6.0E-02 | 1 | ||
| rs1905675 | 1.000 | 0.040 | 12 | 30538874 | intergenic variant | G/A | snv | 0.53 | 1 | ||
| rs1926283 | 1.000 | 0.040 | 1 | 67982978 | intron variant | A/G;T | snv | 1 | |||
| rs2065970 | 1.000 | 0.040 | 1 | 25725032 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs222723 | 1.000 | 0.040 | 14 | 23629422 | upstream gene variant | C/T | snv | 0.74 | 1 | ||
| rs2682665 | 1.000 | 0.040 | 8 | 13940496 | intergenic variant | C/A;T | snv | 1 | |||
| rs2948491 | 1.000 | 0.040 | X | 40321436 | intergenic variant | C/T | snv | 8.1E-02 | 1 | ||
| rs35062843 | 1.000 | 0.040 | 17 | 16948892 | synonymous variant | A/C | snv | 4.2E-02 | 3.6E-02 | 1 | |
| rs356086 | 1.000 | 0.040 | 1 | 55528629 | intron variant | A/G | snv | 7.1E-02 | 1 | ||
| rs375099 | 1.000 | 0.040 | 2 | 109043821 | intergenic variant | G/A;C | snv | 1 | |||
| rs4299072 | 1.000 | 0.040 | 14 | 65238540 | intron variant | G/A | snv | 7.0E-02 | 1 | ||
| rs4592938 | 1.000 | 0.040 | 21 | 45232575 | upstream gene variant | G/A | snv | 9.1E-02 | 1 | ||
| rs4765961 | 1.000 | 0.040 | 12 | 2559306 | intron variant | T/C;G | snv | 1 | |||
| rs5918500 | 1.000 | 0.040 | X | 38209996 | intron variant | C/T | snv | 1 | |||
| rs5925651 | 1.000 | 0.040 | X | 22651114 | intron variant | C/A | snv | 0.24 | 1 | ||
| rs5977837 | 1.000 | 0.040 | X | 133235903 | downstream gene variant | T/C | snv | 0.11 | 1 | ||
| rs5987017 | 1.000 | 0.040 | X | 153516714 | upstream gene variant | A/G | snv | 1 | |||
| rs6649722 | 1.000 | 0.040 | X | 144310656 | upstream gene variant | C/T | snv | 4.0E-02 | 1 | ||
| rs7280675 | 1.000 | 0.040 | 21 | 17898627 | upstream gene variant | T/G | snv | 8.2E-02 | 1 |