| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7914926 | 10 | 79170941 | intron variant | A/G | snv | 0.41 | 1 | ||||
| rs703984 | 10 | 79181660 | intron variant | G/C;T | snv | 1 | |||||
| rs77911174 | 0.925 | 0.080 | 10 | 79067076 | intron variant | A/G | snv | 5.4E-02 | 1 | ||
| rs704010 | 0.851 | 0.080 | 10 | 79081391 | intron variant | T/C | snv | 0.71 | 1 | ||
| rs1268974 | 1.000 | 0.080 | 10 | 79092621 | intron variant | A/G | snv | 0.65 | 1 | ||
| rs2802372 | 10 | 79287818 | intron variant | A/C | snv | 0.44 | 1 | ||||
| rs10128264 | 1.000 | 0.120 | 10 | 79200216 | intron variant | T/C | snv | 0.64 | 1 | ||
| rs74142329 | 10 | 79190231 | intron variant | C/T | snv | 4.9E-02 | 1 |