| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
| rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
| rs35424040 | 0.827 | 0.080 | 11 | 5226940 | missense variant | C/A;G;T | snv | 1.2E-05 | 6 | ||
| rs35152987 | 0.925 | 0.080 | 11 | 5234352 | missense variant | C/A;T | snv | 2.2E-03 | 4 | ||
| rs1355384700 | 1.000 | 0.080 | 9 | 89405447 | missense variant | A/C | snv | 8.0E-06 | 1 |