Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1257401983 | 1.000 | 0.120 | 17 | 61744445 | stop gained | G/C | snv | 3 | |||
rs273898674 | 0.925 | 0.200 | 17 | 43093472 | stop gained | G/A | snv | 3 | |||
rs397507828 | 1.000 | 13 | 32340440 | stop gained | G/T | snv | 3 | ||||
rs398122630 | 0.925 | 0.200 | 17 | 43094204 | stop gained | T/A | snv | 3 | |||
rs771203198 | 0.925 | 0.200 | 13 | 32394750 | stop gained | G/A;C | snv | 4.0E-06 | 3 | ||
rs80359222 | 0.925 | 0.200 | 13 | 32394913 | stop gained | A/G;T | snv | 3 | |||
rs876659036 | 1.000 | 0.080 | 16 | 23622997 | stop gained | C/A;G | snv | 8.0E-06; 8.0E-06 | 3 | ||
rs886037802 | 0.925 | 0.200 | 13 | 32339561 | stop gained | C/G;T | snv | 3 | |||
rs1057518638 | 1.000 | 13 | 32339317 | stop gained | T/A | snv | 2 | ||||
rs1131692035 | 1.000 | 13 | 32332335 | stop gained | C/G | snv | 2 | ||||
rs1555283169 | 1.000 | 13 | 32337677 | stop gained | A/T | snv | 2 | ||||
rs1555599208 | 1.000 | 17 | 43115726 | stop gained | TTGCAAAATATGTGGTCACACTTTGTGGAGACAGGTTCCTTGATCAACTCCAGA/- | del | 2 | ||||
rs397507649 | 1.000 | 13 | 32337345 | stop gained | T/A;G | snv | 2 | ||||
rs397507967 | 1.000 | 13 | 32363397 | stop gained | T/A;G | snv | 2 | ||||
rs397508983 | 1.000 | 17 | 43092959 | stop gained | G/A;C | snv | 4.0E-06 | 2 | |||
rs397509160 | 1.000 | 17 | 43082474 | stop gained | G/A;T | snv | 2 | ||||
rs80357167 | 1.000 | 17 | 43094066 | stop gained | C/A;T | snv | 2 | ||||
rs886037787 | 1.000 | 17 | 43092961 | stop gained | A/T | snv | 2 | ||||
rs1131692162 | 17 | 43099781 | stop gained | C/A | snv | 1 | |||||
rs1553622530 | 2 | 214781220 | stop gained | C/T | snv | 1 | |||||
rs1554897879 | 10 | 87931085 | stop gained | C/A | snv | 1 | |||||
rs1555114766 | 11 | 108317486 | stop gained | G/A | snv | 1 | |||||
rs1555461693 | 16 | 23635903 | stop gained | C/A | snv | 1 | |||||
rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;G;T | snv | 52 | |||
rs121913279 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 45 |