Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13247874 | 7 | 73596112 | intron variant | C/T | snv | 0.15 | 0.15 | 1 | |||
rs11075253 | 16 | 15054789 | intron variant | C/A | snv | 0.22 | 1 | ||||
rs186183604 | 11 | 67361262 | intron variant | G/A;T | snv | 1 |