| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13427836 | 1.000 | 0.040 | 2 | 128270387 | intron variant | C/T | snv | 0.11 | 2 | ||
| rs11574 | 1.000 | 0.040 | 1 | 23559007 | missense variant | T/A;C | snv | 0.80 | 2 | ||
| rs6777038 | 1.000 | 0.040 | 3 | 185723172 | intron variant | C/T | snv | 0.11 | 2 | ||
| rs2276048 | 1.000 | 0.040 | 11 | 72230168 | synonymous variant | A/G | snv | 0.24 | 0.28 | 2 | |
| rs2299620 | 1.000 | 0.040 | 11 | 2837065 | intron variant | C/T | snv | 0.11 | 2 | ||
| rs867120336 | 1.000 | 0.040 | 2 | 10048589 | frameshift variant | -/A | delins | 4.1E-06 | 2 | ||
| rs931891 | 1.000 | 0.040 | 15 | 97749977 | intron variant | C/A | snv | 6.4E-02 | 2 | ||
| rs10497721 | 1.000 | 0.040 | 2 | 192049636 | intron variant | C/A;T | snv | 2 | |||
| rs59014890 | 1.000 | 0.040 | 2 | 21286220 | intron variant | T/C | snv | 0.27 | 2 | ||
| rs59825600 | 1.000 | 0.040 | 1 | 14806568 | intron variant | G/A | snv | 0.11 | 2 | ||
| rs3087684 | 1.000 | 0.040 | 3 | 57272291 | 3 prime UTR variant | T/C | snv | 0.67 | 2 | ||
| rs10484821 | 1.000 | 0.040 | 6 | 139547773 | intron variant | T/C | snv | 0.15 | 2 | ||
| rs4394754 | 1.000 | 0.040 | 10 | 132529558 | intergenic variant | T/C;G | snv | 2 | |||
| rs9299870 | 1.000 | 0.040 | 10 | 129471045 | intron variant | C/A;G;T | snv | 2 | |||
| rs7935082 | 1.000 | 0.040 | 11 | 60387527 | intron variant | T/C | snv | 0.62 | 2 | ||
| rs5756152 | 1.000 | 0.040 | 22 | 36316427 | intron variant | A/G | snv | 0.90 | 2 | ||
| rs1036915 | 1.000 | 0.040 | 9 | 84822934 | intron variant | A/G | snv | 0.40 | 2 | ||
| rs1187274 | 1.000 | 0.040 | 9 | 84804874 | intron variant | C/G | snv | 0.55 | 2 | ||
| rs199976415 | 1.000 | 0.040 | 1 | 26911982 | missense variant | G/A | snv | 6.0E-05 | 2.1E-05 | 2 | |
| rs2284912 | 1.000 | 0.040 | 20 | 17457568 | intron variant | T/C | snv | 1.7E-02 | 2 | ||
| rs6044695 | 1.000 | 0.040 | 20 | 17244293 | intron variant | A/T | snv | 0.41 | 2 | ||
| rs952635 | 1.000 | 0.040 | 1 | 66226202 | intron variant | C/G;T | snv | 2 | |||
| rs143517122 | 1.000 | 0.040 | 13 | 27924267 | missense variant | G/A;T | snv | 2.1E-04; 4.2E-06 | 2 | ||
| rs372098146 | 1.000 | 0.040 | 21 | 43753698 | missense variant | C/A;G | snv | 4.0E-06; 2.8E-05 | 2 | ||
| rs377592729 | 1.000 | 0.040 | 21 | 43748998 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 2 |