Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs886041095 | 0.827 | 0.160 | 12 | 13571930 | missense variant | C/T | snv | 11 | |||
rs869312704 | 0.882 | 0.160 | 2 | 161423752 | frameshift variant | -/GGCTGCA | delins | 10 | |||
rs1554297905 | 0.882 | 0.160 | 7 | 39686740 | missense variant | G/A | snv | 6 | |||
rs869312689 | 0.925 | 0.160 | 1 | 244053934 | missense variant | T/C | snv | 5 | |||
rs767961672 | 0.925 | 0.200 | 14 | 28767822 | missense variant | G/A;T | snv | 4.0E-06 | 4 | ||
rs869312707 | 0.925 | 0.160 | 12 | 115963422 | missense variant | G/A | snv | 4 | |||
rs869312660 | 0.925 | 0.160 | X | 72488932 | splice donor variant | C/T | snv | 3 |