Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs796052505 | 0.724 | 0.440 | 5 | 162095551 | missense variant | G/A;C | snv | 57 | |||
rs80338945 | 0.695 | 0.440 | 13 | 20189313 | missense variant | A/G | snv | 6.4E-04 | 6.4E-04 | 32 | |
rs387907141 | 0.752 | 0.360 | 6 | 157181137 | stop gained | C/T | snv | 24 | |||
rs1558373252 | 0.790 | 0.120 | 2 | 5693013 | frameshift variant | T/- | delins | 19 | |||
rs1553212868 | 0.807 | 0.280 | 1 | 151406264 | frameshift variant | G/- | delins | 17 | |||
rs1555528356 | 0.790 | 0.360 | 16 | 89282836 | stop gained | G/A | snv | 13 | |||
rs794727774 | 0.827 | 0.240 | 1 | 23848684 | stop gained | C/T | snv | 11 | |||
rs1334099693 | 0.882 | 0.080 | 6 | 21594732 | missense variant | C/A;T | snv | 4.6E-06 | 11 | ||
rs1057516044 | 0.851 | 0.240 | 12 | 21913005 | missense variant | A/G | snv | 9 | |||
rs1131691804 | 0.807 | 0.200 | 15 | 48463123 | missense variant | G/A | snv | 8 | |||
rs397507481 | 0.882 | 0.240 | 7 | 140754206 | missense variant | G/C;T | snv | 4 |