Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 47 | ||
| rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
| rs150813342 | 9 | 132989126 | synonymous variant | C/T | snv | 4.1E-03 | 4.1E-03 | 9 | |||
| rs11553699 | 12 | 121779004 | 3 prime UTR variant | A/G | snv | 9.4E-02 | 6 | ||||
| rs1434282 | 1 | 199041592 | non coding transcript exon variant | C/T | snv | 0.76 | 6 | ||||
| rs1354034 | 3 | 56815721 | intron variant | T/C | snv | 0.49 | 4 | ||||
| rs56043070 | 1 | 247556467 | splice donor variant | G/A;T | snv | 5.2E-02; 4.1E-06 | 4 | ||||
| rs139141690 | 7 | 101856650 | intron variant | G/A | snv | 2.2E-03 | 3 | ||||
| rs34950321 | 5 | 76668682 | missense variant | C/T | snv | 1.7E-02 | 1.6E-02 | 3 | |||
| rs649729 | 1.000 | 0.040 | 2 | 31241519 | intron variant | T/A;C | snv | 3 | |||
| rs1339847 | 1 | 247875992 | missense variant | G/A | snv | 0.12 | 0.10 | 2 | |||
| rs17853159 | 1 | 45345193 | missense variant | G/A | snv | 5.2E-02 | 5.1E-02 | 2 |