| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs66519732 | 4 | 6988842 | intron variant | C/G;T | snv | 2 | |||||
| rs10013696 | 4 | 6977000 | intron variant | A/G | snv | 0.45 | 1 | ||||
| rs116383353 | 4 | 6923070 | intron variant | G/A;T | snv | 1 | |||||
| rs6831368 | 4 | 6968192 | intron variant | A/C;G | snv | 1 | |||||
| rs12119 | 4 | 7031944 | 3 prime UTR variant | C/G;T | snv | 0.45 | 1 |