| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2218400 | 1.000 | 0.120 | 13 | 63564941 | intergenic variant | C/A | snv | 0.34 | 1 | ||
| rs2417487 | 1.000 | 0.120 | 9 | 104125300 | intron variant | A/G;T | snv | 1 | |||
| rs2900174 | 1.000 | 0.120 | 12 | 11394598 | intron variant | A/G | snv | 0.12 | 1 | ||
| rs351365 | 1.000 | 0.120 | 1 | 112503773 | intron variant | T/C;G | snv | 1 | |||
| rs361052 | 1.000 | 0.120 | 3 | 13029299 | intron variant | A/G | snv | 0.73 | 1 | ||
| rs375328708 | 1.000 | 0.120 | 19 | 1226602 | synonymous variant | C/G;T | snv | 6.7E-05 | 6.3E-05 | 1 | |
| rs387906389 | 1.000 | 0.120 | 12 | 51986840 | frameshift variant | GATGA/- | del | 1 | |||
| rs397518442 | 1.000 | 0.120 | 19 | 1220630 | frameshift variant | C/- | delins | 1 | |||
| rs4285214 | 1.000 | 0.120 | 5 | 124688588 | intron variant | T/G | snv | 0.55 | 1 | ||
| rs450960 | 1.000 | 0.120 | 22 | 17833538 | intron variant | C/T | snv | 0.30 | 1 | ||
| rs6073450 | 1.000 | 0.120 | 20 | 44458008 | intron variant | G/A | snv | 0.43 | 1 | ||
| rs6537481 | 1.000 | 0.120 | 4 | 147474942 | intergenic variant | A/C;G | snv | 1 | |||
| rs6662005 | 1.000 | 0.120 | 1 | 236276616 | intron variant | G/A | snv | 0.16 | 1 | ||
| rs6971499 | 1.000 | 0.120 | 7 | 130995762 | intron variant | T/C | snv | 0.15 | 1 | ||
| rs7190458 | 1.000 | 0.120 | 16 | 75229763 | synonymous variant | G/A | snv | 5.1E-02 | 0.11 | 1 | |
| rs7214041 | 1.000 | 0.120 | 17 | 72405335 | intron variant | C/T | snv | 0.17 | 1 | ||
| rs7330800 | 1.000 | 0.120 | 13 | 63573938 | intergenic variant | A/C;T | snv | 1 | |||
| rs73328514 | 1.000 | 0.120 | 7 | 47448971 | intron variant | A/T | snv | 0.15 | 1 | ||
| rs77038344 | 1.000 | 0.120 | 17 | 40487962 | intron variant | C/T | snv | 8.4E-02 | 1 | ||
| rs9554197 | 1.000 | 0.120 | 13 | 27902841 | intron variant | C/T | snv | 0.34 | 1 | ||
| rs9581943 | 1.000 | 0.120 | 13 | 27919860 | upstream gene variant | G/A | snv | 0.31 | 1 | ||
| rs962856 | 1.000 | 0.120 | 2 | 67366671 | intron variant | C/T | snv | 0.66 | 1 | ||
| rs981621 | 1.000 | 0.120 | 18 | 13357201 | intron variant | A/C;G | snv | 0.40 | 1 | ||
| rs1049074086 | 0.925 | 0.120 | 11 | 1759567 | missense variant | A/G | snv | 7.0E-06 | 9 | ||
| rs7310409 | 0.925 | 0.160 | 12 | 120987058 | intron variant | A/C;G;T | snv | 7 |