| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs9257809 | 0.790 | 0.320 | 6 | 29388554 | intron variant | A/G | snv | 5.8E-02 | 4 | ||
| rs3749971 | 0.925 | 0.160 | 6 | 29374998 | missense variant | G/A | snv | 5.5E-02 | 5.7E-02 | 3 | |
| rs3094548 | 6 | 29387425 | intron variant | G/A;C | snv | 2 | |||||
| rs7753474 | 1.000 | 0.120 | 6 | 29373531 | 3 prime UTR variant | G/A | snv | 0.22 | 1 | ||
| rs3117440 | 6 | 29373889 | 3 prime UTR variant | T/A | snv | 0.95 | 1 |