| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7341475 | 0.851 | 0.240 | 7 | 103764368 | intron variant | G/A | snv | 0.17 | 2 | ||
| rs17606561 | 1.000 | 0.040 | 6 | 10982126 | 3 prime UTR variant | G/A | snv | 0.17 | 1 | ||
| rs3756963 | 0.882 | 0.200 | 6 | 11021921 | intron variant | T/C | snv | 0.24 | 1 | ||
| rs10498676 | 0.925 | 0.040 | 6 | 11026766 | intron variant | G/A | snv | 0.18 | 1 | ||
| rs9468304 | 1.000 | 0.040 | 6 | 11041932 | intron variant | G/A | snv | 0.19 | 1 | ||
| rs1858830 | 0.925 | 0.040 | 7 | 116672385 | 5 prime UTR variant | C/G | snv | 0.40 | 1 | ||
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 6 | |
| rs1565532385 | 0.925 | 0.080 | 11 | 118374964 | frameshift variant | CA/- | del | 3 | |||
| rs375712202 | 1.000 | 0.040 | 11 | 124923339 | splice donor variant | C/T | snv | 9.6E-05 | 1.4E-05 | 1 | |
| rs886037776 | 0.925 | 0.280 | 9 | 137817477 | stop gained | G/A | snv | 2 | |||
| rs11787216 | 1.000 | 0.040 | 8 | 141605122 | intron variant | C/T | snv | 0.26 | 2 | ||
| rs4534 | 0.925 | 0.240 | 8 | 142879686 | missense variant | C/T | snv | 8.4E-02 | 4.1E-02 | 1 | |
| rs7794745 | 0.851 | 0.040 | 7 | 146792514 | intron variant | A/T | snv | 0.49 | 1 | ||
| rs1396313317 | 1.000 | 0.040 | 7 | 147562137 | splice acceptor variant | G/A;C | snv | 4.0E-06 | 1 | ||
| rs4141463 | 0.925 | 0.040 | 20 | 14766825 | intron variant | T/C | snv | 0.50 | 1 | ||
| rs2710102 | 0.790 | 0.120 | 7 | 147877298 | intron variant | A/G;T | snv | 1 | |||
| rs121908445 | 0.925 | 0.040 | 7 | 148147542 | missense variant | T/C | snv | 3.3E-04 | 1.7E-04 | 1 | |
| rs121912562 | 0.925 | 0.160 | 4 | 148435252 | stop gained | G/A;C | snv | 4.0E-06 | 2 | ||
| rs1553518509 | 1.000 | 0.040 | 2 | 148468916 | stop gained | C/T | snv | 2 | |||
| rs10741657 | 0.637 | 0.520 | 11 | 14893332 | upstream gene variant | A/G | snv | 0.65 | 3 | ||
| rs1452048149 | 1.000 | 0.040 | 1 | 151404828 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs370498156 | 1.000 | 0.040 | 1 | 151404903 | missense variant | T/C;G | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs756691187 | 1.000 | 0.040 | 1 | 151404993 | missense variant | C/G | snv | 8.0E-06 | 7.0E-06 | 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 |