| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
| rs11172113 | 0.882 | 0.080 | 12 | 57133500 | intron variant | T/C | snv | 0.42 | 10 | ||
| rs1529672 | 1.000 | 0.040 | 3 | 25479091 | intron variant | C/A;T | snv | 6 | |||
| rs2798641 | 6 | 108946847 | intron variant | C/T | snv | 0.15 | 5 | ||||
| rs8089099 | 18 | 10078074 | regulatory region variant | G/A | snv | 0.22 | 3 |