Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519953 | 0.807 | 0.200 | 3 | 49375576 | missense variant | C/A;T | snv | 3 | |||
rs146054764 | 0.882 | 0.160 | 1 | 15506000 | missense variant | T/G | snv | 1.4E-03; 8.0E-06 | 1.4E-03 | 4 | |
rs352140 | 0.630 | 0.680 | 3 | 52222681 | synonymous variant | C/A;G;T | snv | 2.0E-05; 0.49 | 41 | ||
rs397518423 | 0.790 | 0.240 | 1 | 9726972 | missense variant | G/A | snv | 6 | |||
rs5743836 | 0.658 | 0.440 | 3 | 52226766 | intron variant | A/G | snv | 0.20 | 31 | ||
rs747141352 | 0.882 | 0.160 | 8 | 127736607 | missense variant | G/A;C | snv | 8.0E-06 | 3 | ||
rs923910999 | 0.882 | 0.160 | 20 | 63667537 | missense variant | A/G | snv | 4.0E-06 | 3 |