| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2814778 | 0.763 | 0.360 | 1 | 159204893 | 5 prime UTR variant | T/C | snv | 0.25 | 3 | ||
| rs6680396 | 1.000 | 0.040 | 1 | 196663340 | intron variant | A/G | snv | 0.22 | 3 | ||
| rs800292 | 0.645 | 0.560 | 1 | 196673103 | missense variant | G/A | snv | 0.32 | 0.40 | 3 | |
| rs9332739 | 0.763 | 0.360 | 6 | 31936027 | missense variant | G/A;C | snv | 4.1E-06; 3.9E-02 | 2 | ||
| rs12049351 | 1 | 229582254 | intergenic variant | C/G | snv | 0.23 | 1 | ||||
| rs12940923 | 17 | 58292488 | intergenic variant | A/T | snv | 0.13 | 1 | ||||
| rs1390943 | 8 | 20224379 | intron variant | T/G | snv | 0.42 | 1 | ||||
| rs505102 | 1 | 196650372 | upstream gene variant | T/C | snv | 0.40 | 1 | ||||
| rs28730837 | 1.000 | 0.080 | 17 | 58278036 | missense variant | G/A | snv | 1.2E-02 | 1.2E-02 | 1 | |
| rs35897051 | 1.000 | 0.080 | 17 | 58270865 | splice acceptor variant | T/G | snv | 4.4E-03 | 4.6E-03 | 1 | |
| rs3134931 | 6 | 32222843 | intron variant | T/C | snv | 0.35 | 0.37 | 1 | |||
| rs9911753 | 17 | 58905813 | intron variant | G/A;T | snv | 1 | |||||
| rs6042507 | 20 | 1478415 | missense variant | T/A;C;G | snv | 9.6E-05; 4.0E-06; 0.91 | 1 | ||||
| rs6503905 | 17 | 59210093 | synonymous variant | A/G | snv | 0.62 | 0.71 | 1 | |||
| rs8081967 | 17 | 58995340 | intron variant | T/A;C | snv | 1 | |||||
| rs2680701 | 17 | 58360940 | missense variant | G/A | snv | 0.14 | 0.14 | 1 |