| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 7 | ||
| rs6028 | 1 | 169582444 | synonymous variant | T/C | snv | 0.29 | 0.23 | 1 | |||
| rs6013 | 1 | 169518583 | intron variant | G/A;T | snv | 2.6E-04; 6.4E-02 | 1 | ||||
| rs1018827 | 1 | 169544768 | intron variant | A/G | snv | 0.92 | 1 | ||||
| rs4524 | 1 | 169542517 | missense variant | T/C | snv | 0.28 | 0.24 | 1 | |||
| rs6427196 | 1.000 | 0.080 | 1 | 169511985 | 3 prime UTR variant | C/G;T | snv | 1 | |||
| rs1557570 | 1 | 169538606 | intron variant | G/T | snv | 0.30 | 1 | ||||
| rs10800453 | 1 | 169537838 | intron variant | T/A | snv | 0.25 | 1 | ||||
| rs9332591 | 1 | 169545552 | intron variant | G/A | snv | 9.5E-02 | 1 | ||||
| rs9332701 | 1 | 169515529 | missense variant | A/G | snv | 3.0E-02 | 3.1E-02 | 1 | |||
| rs1800594 | 1 | 169541286 | synonymous variant | A/G | snv | 0.34 | 0.34 | 1 | |||
| rs966751 | 1 | 169516903 | intron variant | C/G | snv | 5.3E-02 | 1 | ||||
| rs9287090 | 1 | 169541142 | synonymous variant | G/A | snv | 0.21 | 0.22 | 1 | |||
| rs2187953 | 1 | 169530143 | intron variant | A/C | snv | 0.24 | 1 | ||||
| rs4525 | 1 | 169542496 | missense variant | T/C | snv | 0.28 | 0.24 | 1 | |||
| rs72708013 | 1 | 169512493 | 3 prime UTR variant | T/G | snv | 5.5E-02 | 1 | ||||
| rs6703865 | 1 | 169581725 | intron variant | G/A | snv | 0.11 | 1 |