| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs35468074 | 9 | 13930482 | intron variant | -/A | delins | 0.11 | 1 | ||||
| rs607900 | 9 | 133340381 | 3 prime UTR variant | T/C | snv | 8.1E-02 | 1 | ||||
| rs3751198 | 12 | 103753429 | intron variant | A/G | snv | 0.59 | 1 | ||||
| rs35108384 | 9 | 133101311 | non coding transcript exon variant | G/A | snv | 0.23 | 0.20 | 1 | |||
| rs11780263 | 8 | 27966315 | intron variant | G/A | snv | 0.19 | 1 | ||||
| rs55829013 | 8 | 27920631 | intron variant | A/C | snv | 0.33 | 1 | ||||
| rs7816579 | 8 | 27948298 | intron variant | A/C;G;T | snv | 1 | |||||
| rs3124758 | 9 | 133479731 | upstream gene variant | G/A;C | snv | 1 | |||||
| rs2723889 | 12 | 103606692 | intron variant | T/C | snv | 0.72 | 1 | ||||
| rs62575992 | 9 | 133389365 | intron variant | C/T | snv | 6.3E-02 | 1 | ||||
| rs9399599 | 6 | 147382163 | intron variant | A/T | snv | 0.51 | 1 | ||||
| rs10498631 | 14 | 91802187 | intron variant | C/T | snv | 0.29 | 1 | ||||
| rs58204830 | 14 | 91836628 | intron variant | G/A | snv | 8.4E-02 | 1 | ||||
| rs150926226 | X | 155491696 | intron variant | G/A;C | snv | 1 | |||||
| rs12423482 | 12 | 5961679 | intron variant | A/G | snv | 4.4E-02 | 1 | ||||
| rs57040304 | 12 | 5953728 | non coding transcript exon variant | A/G | snv | 9.7E-02 | 1 | ||||
| rs7135039 | 12 | 6051448 | intron variant | C/T | snv | 0.40 | 1 |