Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387906659 | 0.742 | 0.280 | 19 | 40257052 | stop gained | C/A;T | snv | 14 | |||
rs749140677 | 0.752 | 0.240 | 12 | 47857185 | missense variant | G/A | snv | 8.0E-06 | 13 | ||
rs771138120 | 0.827 | 0.120 | 9 | 21971191 | missense variant | G/A;C;T | snv | 9.1E-06; 4.5E-06 | 13 | ||
rs121913514 | 0.763 | 0.240 | 4 | 54733174 | missense variant | T/A;G | snv | 12 | |||
rs121913521 | 0.790 | 0.120 | 4 | 54727447 | missense variant | T/A;C;G | snv | 12 |