| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17597773 | 1 | 220881419 | non coding transcript exon variant | C/G | snv | 0.25 | 0.23 | 2 | |||
| rs2184658 | 0.925 | 0.120 | 1 | 220879115 | intron variant | C/G | snv | 0.20 | 2 | ||
| rs41369048 | 1 | 220878224 | intron variant | A/G | snv | 9.7E-02 | 2 | ||||
| rs12037861 | 1 | 220864835 | intron variant | A/T | snv | 0.28 | 1 | ||||
| rs2131887 | 1.000 | 0.040 | 1 | 220834513 | intron variant | T/C | snv | 0.61 | 1 | ||
| rs2453237 | 1 | 220855242 | intron variant | G/A;T | snv | 1 | |||||
| rs12141189 | 1 | 220880203 | missense variant | T/C | snv | 0.24 | 0.23 | 1 |