| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10858583 | 1.000 | 0.040 | 12 | 87334666 | intergenic variant | C/T | snv | 0.79 | 3 | ||
| rs12149074 | 1.000 | 0.040 | 16 | 80071969 | intron variant | C/A;G | snv | 3 | |||
| rs13086738 | 1.000 | 0.040 | 3 | 181080939 | intron variant | A/G | snv | 0.21 | 3 | ||
| rs1805576 | 1.000 | 0.040 | 3 | 180949777 | intron variant | C/G;T | snv | 0.24 | 3 | ||
| rs4148087 | 1.000 | 0.040 | 21 | 42202157 | intron variant | G/A;T | snv | 3 | |||
| rs4854912 | 1.000 | 0.040 | 3 | 181063312 | intron variant | C/T | snv | 0.15 | 3 |