| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12050217 | 0.827 | 0.160 | 14 | 96262416 | intron variant | A/G | snv | 0.21 | 6 | ||
| rs12150053 | 1.000 | 0.120 | 17 | 1761175 | upstream gene variant | T/A;C | snv | 1 | |||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs12219125 | 0.925 | 0.120 | 10 | 20304158 | intergenic variant | G/T | snv | 0.15 | 2 | ||
| rs12267418 | 0.882 | 0.280 | 10 | 19425625 | intron variant | G/A | snv | 0.18 | 3 | ||
| rs1232898090 | 0.637 | 0.600 | 22 | 46198429 | missense variant | G/C;T | snv | 4.0E-06; 4.0E-06 | 40 | ||
| rs1241356540 | 0.851 | 0.160 | 17 | 63497137 | missense variant | C/T | snv | 5 | |||
| rs1243046808 | 0.925 | 0.160 | 6 | 43770758 | missense variant | C/G;T | snv | 2.0E-05; 9.8E-06 | 2 | ||
| rs1249719 | 1.000 | 0.120 | 9 | 114235944 | intron variant | G/A | snv | 6.8E-02 | 2 | ||
| rs12656571 | 1.000 | 0.120 | 5 | 109742339 | intron variant | G/A | snv | 0.17 | 1 | ||
| rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
| rs12948385 | 1.000 | 0.120 | 17 | 1761607 | upstream gene variant | G/A | snv | 0.26 | 1 | ||
| rs13064954 | 1.000 | 0.120 | 3 | 157136953 | downstream gene variant | G/A | snv | 7.9E-02 | 1 | ||
| rs13163610 | 1.000 | 0.120 | 5 | 94213172 | intron variant | A/C | snv | 0.11 | 1 | ||
| rs13207351 | 0.851 | 0.280 | 6 | 43770057 | upstream gene variant | A/G;T | snv | 4 | |||
| rs1372503923 | 0.925 | 0.160 | 5 | 53048731 | missense variant | A/C | snv | 3 | |||
| rs1373054855 | 1.000 | 0.120 | 17 | 64370017 | missense variant | A/G | snv | 1.4E-05 | 1 | ||
| rs139876191 | 1.000 | 0.120 | 6 | 34242693 | intron variant | -/C | delins | 7.7E-02; 5.8E-06 | 5.2E-02 | 1 | |
| rs1400094618 | 0.882 | 0.240 | 14 | 102229508 | missense variant | A/G | snv | 3 | |||
| rs140421861 | 1.000 | 0.120 | 4 | 73413512 | synonymous variant | C/T | snv | 1.1E-04 | 1.1E-04 | 1 | |
| rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
| rs142293996 | 1.000 | 0.120 | 1 | 224260357 | intron variant | C/A | snv | 1.1E-02 | 1 | ||
| rs14259 | 0.724 | 0.360 | 12 | 121915890 | missense variant | A/C;G | snv | 4.0E-06; 0.32 | 19 | ||
| rs142610219 | 1.000 | 0.120 | 8 | 115906039 | intergenic variant | A/T | snv | 2.7E-03 | 1 | ||
| rs148995025 | 1.000 | 0.120 | 5 | 7085094 | intron variant | A/G | snv | 8.9E-03 | 1 |