Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs66548636 | 0.925 | 0.120 | 17 | 50195469 | missense variant | C/A;G;T | snv | 2 | |||
rs67507747 | 0.827 | 0.160 | 17 | 50194032 | missense variant | C/A;G;T | snv | 5 | |||
rs67771061 | 0.925 | 0.120 | 17 | 50188776 | missense variant | C/A;G;T | snv | 2 | |||
rs72645315 | 0.925 | 0.120 | 17 | 50197205 | missense variant | C/T | snv | 2 | |||
rs72654802 | 0.882 | 0.120 | 17 | 50188122 | missense variant | C/T | snv | 3 | |||
rs72656343 | 0.882 | 0.120 | 17 | 50186386 | stop gained | C/A;T | snv | 3 | |||
rs72659305 | 0.925 | 0.120 | 7 | 94425127 | missense variant | G/A | snv | 2 |