Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1805087 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 135 | |
rs766958673 | 0.851 | 0.120 | 21 | 43066293 | missense variant | C/G;T | snv | 4.0E-06 | 4 | ||
rs746782366 | 0.925 | 0.120 | 21 | 43072117 | missense variant | C/G;T | snv | 8.1E-06; 4.0E-06 | 2 | ||
rs756065494 | 0.925 | 0.120 | 1 | 236835605 | missense variant | A/G | snv | 2.8E-05 | 2 |