Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057518843 | 0.790 | 0.240 | 14 | 87988523 | missense variant | C/T | snv | 19 | |||
rs886041091 | 0.807 | 0.120 | 9 | 84751990 | missense variant | A/G | snv | 18 | |||
rs386834061 | 0.925 | 0.360 | 8 | 99868312 | stop gained | C/T | snv | 2.1E-05 | 10 | ||
rs864309505 | 0.807 | 0.200 | 11 | 6615220 | missense variant | T/G | snv | 10 | |||
rs1057518939 | 1.000 | 0.040 | 8 | 99511424 | frameshift variant | A/- | del | 9 | |||
rs1561416879 | 0.925 | 0.200 | 5 | 90629308 | stop gained | C/G | snv | 6 | |||
rs1564855725 | 0.882 | 0.160 | 11 | 6617621 | splice region variant | C/T | snv | 5 | |||
rs606231180 | 0.925 | 0.080 | X | 38285902 | frameshift variant | CC/- | delins | 3 | |||
rs377274761 | 0.776 | 0.240 | 14 | 87968393 | missense variant | C/T | snv | 8.0E-06 | 2.8E-05 | 20 | |
rs61750420 | 0.689 | 0.480 | 7 | 92501562 | missense variant | C/T | snv | 3.2E-04 | 3.5E-04 | 52 | |
rs142285818 | 0.807 | 0.120 | 3 | 129532727 | missense variant | C/G;T | snv | 9.7E-04 | 4.1E-04 | 11 |