| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12979860 | 0.547 | 0.520 | 19 | 39248147 | intron variant | C/T | snv | 0.39 | 84 | ||
| rs3745274 | 0.672 | 0.480 | 19 | 41006936 | missense variant | G/A;T | snv | 4.0E-06; 0.27 | 30 | ||
| rs28399499 | 0.827 | 0.280 | 19 | 41012316 | missense variant | T/C | snv | 5.1E-03 | 2.2E-02 | 6 | |
| rs1385129 | 1.000 | 1 | 42943295 | synonymous variant | G/A;C | snv | 0.24; 4.0E-06 | 1 | |||
| rs7127617 | 1.000 | 11 | 5680770 | intron variant | G/A | snv | 0.53 | 1 |