Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519522 | 1.000 | 10 | 129877788 | stop gained | G/A | snv | 2 | ||||
rs1057519518 | 1.000 | 10 | 129963462 | missense variant | T/C | snv | 1 | ||||
rs1057519519 | 1.000 | 10 | 129958997 | missense variant | T/C | snv | 1 | ||||
rs1057519520 | 1.000 | 10 | 129877825 | missense variant | C/A | snv | 1 | ||||
rs1554904330 | 1.000 | 10 | 129877811 | missense variant | C/T | snv | 1 | ||||
rs1554934855 | 1.000 | 10 | 129957258 | missense variant | C/T | snv | 1 | ||||
rs1564927062 | 1.000 | 10 | 129958957 | missense variant | CA/AG | mnv | 1 | ||||
rs779003155 | 1.000 | 10 | 129877779 | missense variant | G/A;T | snv | 4.0E-06 | 1 | |||
rs869312668 | 1.000 | 10 | 129957282 | missense variant | G/A | snv | 1 | ||||
rs1057519521 | 0.851 | 0.120 | 10 | 129963375 | frameshift variant | TCTC/- | del | 8 | |||
rs1057519437 | 0.851 | 0.240 | 10 | 129957300 | missense variant | C/T | snv | 6 | |||
rs1057519389 | 0.695 | 0.400 | 10 | 129957324 | missense variant | C/A;G;T | snv | 46 |