| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs16976358 | 0.827 | 0.080 | 18 | 42611606 | intron variant | T/C | snv | 1.0E-02 | 1 | ||
| rs10497655 | 1.000 | 0.040 | 2 | 184597314 | intron variant | T/C;G | snv | 1 | |||
| rs375712202 | 1.000 | 0.040 | 11 | 124923339 | splice donor variant | C/T | snv | 9.6E-05 | 1.4E-05 | 1 | |
| rs4141463 | 0.925 | 0.040 | 20 | 14766825 | intron variant | T/C | snv | 0.50 | 1 | ||
| rs587777457 | 0.925 | 0.200 | X | 43731695 | missense variant | G/T | snv | 1 | |||
| rs61753971 | 0.925 | 0.120 | X | 154030546 | missense variant | C/T | snv | 1.3E-04 | 1.1E-04 | 1 | |
| rs1561824498 | 1.000 | 0.040 | 5 | 88752044 | splice acceptor variant | C/A | snv | 1 | |||
| rs796052733 | 1.000 | 0.040 | 5 | 88731773 | stop gained | G/A | snv | 1 | |||
| rs1858830 | 0.925 | 0.040 | 7 | 116672385 | 5 prime UTR variant | C/G | snv | 0.40 | 1 | ||
| rs762735676 | 1.000 | 0.040 | 17 | 31221945 | frameshift variant | TTT/-;TTTT | delins | 6.6E-05 | 1 | ||
| rs878853147 | 0.925 | 0.200 | X | 71169399 | missense variant | C/T | snv | 1 | |||
| rs1276388879 | 1.000 | 0.040 | 1 | 151405647 | missense variant | A/C;G | snv | 1 | |||
| rs1372713010 | 1.000 | 0.040 | 1 | 151428041 | missense variant | G/A | snv | 1 | |||
| rs1418634444 | 1.000 | 0.040 | 1 | 151408777 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs1452048149 | 1.000 | 0.040 | 1 | 151404828 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs1476293577 | 1.000 | 0.040 | 1 | 151428188 | missense variant | G/A;C | snv | 1 | |||
| rs1484207450 | 1.000 | 0.040 | 1 | 151405155 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs1557863430 | 1.000 | 0.040 | 1 | 151405229 | missense variant | T/C | snv | 1 | |||
| rs1557863440 | 1.000 | 0.040 | 1 | 151405233 | missense variant | T/C | snv | 1 | |||
| rs1557863546 | 1.000 | 0.040 | 1 | 151405263 | missense variant | T/A | snv | 1 | |||
| rs1557867853 | 1.000 | 0.040 | 1 | 151406330 | missense variant | G/A | snv | 1 | |||
| rs1557870645 | 1.000 | 0.040 | 1 | 151407271 | missense variant | C/T | snv | 1 | |||
| rs1557874046 | 1.000 | 0.040 | 1 | 151408807 | missense variant | T/G | snv | 1 | |||
| rs1557901347 | 1.000 | 0.040 | 1 | 151424027 | missense variant | G/C | snv | 1 | |||
| rs1557902023 | 1.000 | 0.040 | 1 | 151424154 | missense variant | G/C | snv | 1 |