| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs16841904 | 0.807 | 0.160 | 1 | 197732862 | intron variant | C/T | snv | 0.18 | 5 | ||
| rs2488389 | 0.925 | 0.040 | 1 | 197662011 | intron variant | G/A | snv | 0.22 | 3 | ||
| rs17641524 | 0.925 | 0.120 | 1 | 197735587 | splice region variant | C/G;T | snv | 4.0E-06; 0.17 | 2 | ||
| rs2488397 | 1.000 | 0.040 | 1 | 197732149 | intron variant | G/C | snv | 0.23 | 2 | ||
| rs2488401 | 1.000 | 0.040 | 1 | 197733271 | intron variant | C/A;T | snv | 1 | |||
| rs2488393 | 1.000 | 0.080 | 1 | 197753110 | intron variant | C/T | snv | 0.23 | 1 | ||
| rs1998598 | 1.000 | 0.040 | 1 | 197758512 | intron variant | A/G;T | snv | 1 | |||
| rs16841842 | 1.000 | 0.040 | 1 | 197642552 | intron variant | C/A | snv | 0.16 | 1 | ||
| rs12118513 | 1.000 | 0.040 | 1 | 197547956 | intron variant | T/A | snv | 0.15 | 1 |