| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs34811474 | 1.000 | 0.040 | 4 | 25407216 | missense variant | G/A;T | snv | 0.15; 4.1E-06 | 8 | ||
| rs1131017 | 0.925 | 0.160 | 12 | 56042145 | 5 prime UTR variant | C/A;G;T | snv | 8.0E-06; 8.0E-06; 0.62; 1.1E-04 | 5 | ||
| rs2764261 | 6 | 108606639 | intron variant | A/G;T | snv | 3 | |||||
| rs17266097 | 2 | 199410486 | intron variant | C/T | snv | 0.29 | 2 | ||||
| rs62023121 | 15 | 92916223 | intron variant | C/T | snv | 0.12 | 2 |