| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10075801 | 5 | 132341949 | intron variant | A/G | snv | 0.31 | 5 | ||||
| rs12777 | 5 | 132335969 | synonymous variant | C/G | snv | 3.1E-02 | 2.8E-02 | 4 | |||
| rs34301845 | 5 | 132329474 | intron variant | TT/-;T;TTT;TTTT;TTTTTTTTTTTTTT | delins | 0.56 | 2 | ||||
| rs272869 | 5 | 132342304 | intron variant | A/G | snv | 0.64 | 2 | ||||
| rs11950562 | 5 | 132316836 | intron variant | A/C | snv | 0.37 | 1 | ||||
| rs10479002 | 5 | 132335969 | synonymous variant | C/G | snv | 1 | |||||
| rs270602 | 5 | 132321007 | intron variant | T/A;C | snv | 1 | |||||
| rs419291 | 5 | 132297662 | intron variant | T/A;C | snv | 1 | |||||
| rs6860806 | 1.000 | 0.080 | 5 | 132304843 | intron variant | A/C;G | snv | 0.46 | 1 | ||
| rs56399423 | 5 | 132336964 | intron variant | T/C | snv | 0.28 | 1 | ||||
| rs1050152 | 0.776 | 0.480 | 5 | 132340627 | missense variant | C/T | snv | 0.29 | 0.28 | 1 | |
| rs538021413 | 5 | 132328824 | intron variant | TATATATATATA/-;TA;TATA;TATATA;TATATATA;TATATATATA;TATATATATATATA;TATATATATATATATA | delins | 0.39 | 1 | ||||
| rs270601 | 5 | 132321304 | intron variant | T/C | snv | 0.71 | 1 | ||||
| rs273909 | 1.000 | 0.040 | 5 | 132331660 | intron variant | A/G | snv | 9.5E-02 | 1 |