Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs1801198 | 0.677 | 0.400 | 22 | 30615623 | missense variant | G/A;C | snv | 5.6E-05; 0.57 | 26 | ||
rs9606756 | 0.790 | 0.160 | 22 | 30610873 | missense variant | A/G | snv | 0.12 | 0.14 | 7 | |
rs3760776 | 0.925 | 0.120 | 19 | 5839735 | upstream gene variant | G/A | snv | 0.22 | 3 |