Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1131690985 | 0.925 | 0.200 | 9 | 95449891 | missense variant | C/T | snv | 3 | |||
rs199476095 | 0.925 | 0.200 | 16 | 2089957 | stop gained | G/A;C | snv | 4.1E-06 | 2 | ||
rs754868200 | 0.925 | 0.200 | 4 | 88052022 | missense variant | A/G | snv | 1.6E-05 | 7.0E-06 | 2 | |
rs35705950 | 0.763 | 0.240 | 11 | 1219991 | splice region variant | G/A;T | snv | 14 | |||
rs121908345 | 0.827 | 0.240 | 22 | 50080391 | missense variant | G/A | snv | 1.3E-04 | 6.3E-05 | 6 | |
rs1364050643 | 0.851 | 0.240 | 2 | 86232711 | missense variant | G/A | snv | 5 |