| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs324420 | 0.637 | 0.440 | 1 | 46405089 | missense variant | C/A | snv | 0.24 | 0.26 | 48 | |
| rs11624704 | 1.000 | 0.080 | 14 | 78319734 | intron variant | A/C | snv | 0.13 | 3 | ||
| rs1004212 | 14 | 78714883 | synonymous variant | C/G;T | snv | 8.0E-06; 0.15 | 2 | ||||
| rs199953844 | 6 | 154039650 | missense variant | C/A;T | snv | 4.0E-06; 1.2E-04 | 2 | ||||
| rs73317305 | 8 | 118486753 | intron variant | T/C | snv | 3.6E-02 | 1 |