| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 174 | |
| rs1805087 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 135 | |
| rs1039659576 | 0.689 | 0.520 | 1 | 236803473 | missense variant | A/G | snv | 21 | |||
| rs63750215 | 0.701 | 0.240 | 1 | 226885603 | missense variant | A/T | snv | 19 | |||
| rs367543041 | 0.742 | 0.200 | 1 | 11022553 | missense variant | G/A;C | snv | 3.0E-05 | 15 | ||
| rs3811463 | 0.752 | 0.400 | 1 | 26427451 | 3 prime UTR variant | T/A;C | snv | 14 | |||
| rs774005786 | 0.790 | 0.080 | 1 | 7970951 | missense variant | G/A;T | snv | 3.9E-04; 2.0E-05 | 8 | ||
| rs28938172 | 0.790 | 0.080 | 1 | 7984981 | missense variant | T/C | snv | 7 | |||
| rs74315355 | 0.790 | 0.080 | 1 | 20644639 | missense variant | G/A | snv | 7 | |||
| rs2153977 | 0.807 | 0.240 | 1 | 113537449 | intron variant | C/T | snv | 0.28 | 6 | ||
| rs4884357 | 0.807 | 0.120 | 1 | 11022301 | missense variant | G/A;T | snv | 4.0E-06 | 6 | ||
| rs538874513 | 0.807 | 0.120 | 1 | 3730017 | missense variant | C/G;T | snv | 8.2E-06; 8.2E-06 | 6 | ||
| rs74315351 | 0.807 | 0.080 | 1 | 7962863 | missense variant | G/A | snv | 6 | |||
| rs74315352 | 0.807 | 0.080 | 1 | 7984930 | missense variant | A/C | snv | 1.4E-04 | 5.9E-04 | 6 | |
| rs6336 | 0.827 | 0.120 | 1 | 156879126 | missense variant | C/T | snv | 4.2E-02 | 3.7E-02 | 5 | |
| rs748343847 | 0.827 | 0.080 | 1 | 20633708 | missense variant | G/A | snv | 6.9E-05 | 5 | ||
| rs2147578 | 0.851 | 0.120 | 1 | 183138564 | non coding transcript exon variant | G/A;C | snv | 4 | |||
| rs2273267 | 0.882 | 0.080 | 1 | 114716848 | upstream gene variant | A/C;T | snv | 4 | |||
| rs34787247 | 0.851 | 0.200 | 1 | 26428582 | 3 prime UTR variant | A/C;G | snv | 4 | |||
| rs3811464 | 0.851 | 0.160 | 1 | 26410652 | upstream gene variant | G/A | snv | 0.42 | 4 | ||
| rs41274458 | 0.851 | 0.080 | 1 | 10303606 | missense variant | G/T | snv | 1.8E-02 | 1.9E-02 | 4 | |
| rs749098599 | 0.882 | 0.080 | 1 | 3683085 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 4 | |
| rs781734330 | 0.851 | 0.080 | 1 | 16995981 | missense variant | C/T | snv | 4 |