| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
| rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
| rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
| rs121912748 | 0.790 | 0.200 | 17 | 44253327 | missense variant | C/T | snv | 4.0E-05 | 2.1E-05 | 9 | |
| rs137853583 | 0.827 | 0.080 | 19 | 34394044 | missense variant | G/A;T | snv | 1.2E-05; 4.0E-06 | 5 | ||
| rs1555366607 | 1.000 | 0.080 | 14 | 64767787 | missense variant | A/G | snv | 5 | |||
| rs2230294 | 0.851 | 0.080 | 19 | 34393927 | missense variant | G/A;T | snv | 2.0E-04 | 4 | ||
| rs121912755 | 0.925 | 0.080 | 17 | 44253150 | missense variant | C/T | snv | 2 | |||
| rs750820522 | 1.000 | 0.080 | 8 | 41688541 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs5035 | 1.000 | 0.080 | 17 | 44261630 | missense variant | T/A;G | snv | 1.2E-05; 3.4E-02 | 1 | ||
| rs755966603 | 1.000 | 0.080 | 1 | 158644315 | synonymous variant | A/G | snv | 4.0E-06 | 1 | ||
| rs1555366592 | 1.000 | 0.080 | 14 | 64767686 | frameshift variant | -/AA | delins | 1 | |||
| rs1566754467 | 1.000 | 0.080 | 14 | 64782493 | stop gained | C/A | snv | 1 |