Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 23 | ||
rs4845604 | 0.776 | 0.200 | 1 | 151829204 | intron variant | G/A;C;T | snv | 10 | |||
rs7725052 | 0.716 | 0.240 | 5 | 40487168 | intron variant | C/T | snv | 0.52 | 15 | ||
rs36051895 | 0.716 | 0.240 | 9 | 4981866 | upstream gene variant | G/T | snv | 0.25 | 15 | ||
rs61839660 | 0.776 | 0.280 | 10 | 6052734 | intron variant | C/T | snv | 5.7E-02 | 9 |