Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137852671 | 0.790 | 0.160 | 11 | 17394295 | missense variant | C/T | snv | 10 | |||
rs146488435 | 0.851 | 0.080 | 17 | 63533914 | missense variant | C/G;T | snv | 8.0E-06; 6.4E-05 | 5 | ||
rs1057518775 | 0.851 | 0.160 | 11 | 17387907 | missense variant | G/A;C | snv | 4 | |||
rs121909730 | 0.882 | 0.040 | 10 | 87053380 | missense variant | G/A | snv | 4 |