| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4625 | 0.716 | 0.280 | 3 | 49534707 | 3 prime UTR variant | A/G | snv | 0.30 | 17 | ||
| rs111327216 | 3 | 49487785 | intron variant | C/T | snv | 0.11 | 1 | ||||
| rs73074811 | 3 | 49516098 | intron variant | A/G;T | snv | 1 | |||||
| rs7647973 | 3 | 49473498 | intron variant | G/A | snv | 0.20 | 1 | ||||
| rs11708955 | 3 | 49502681 | intron variant | T/C;G | snv | 1 |