Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1085307993 | 0.716 | 0.440 | 5 | 161331056 | missense variant | C/T | snv | 53 | |||
rs1554093884 | 1.000 | 5 | 161331014 | missense variant | C/T | snv | 1 | ||||
rs1554093885 | 1.000 | 5 | 161331052 | missense variant | T/C | snv | 1 | ||||
rs1554093894 | 1.000 | 5 | 161331101 | missense variant | T/G | snv | 1 | ||||
rs1554094145 | 1.000 | 5 | 161334754 | missense variant | A/G | snv | 1 | ||||
rs1554094149 | 1.000 | 5 | 161334854 | missense variant | A/G | snv | 1 | ||||
rs606231468 | 1.000 | 5 | 161545228 | missense variant | A/G | snv | 1 |