Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs74315510 | 0.925 | 0.240 | 22 | 50524255 | stop gained | G/A | snv | 8.4E-05 | 3.5E-05 | 2 | |
rs121908508 | 1.000 | 0.200 | 22 | 50524305 | stop gained | C/A;T | snv | 1 | |||
rs74315512 | 1.000 | 0.200 | 22 | 50524144 | stop gained | G/A | snv | 1.6E-05 | 1 | ||
rs1064792875 | 1.000 | 22 | 50525908 | stop gained | C/T | snv | 1 | ||||
rs866001342 | 1.000 | 22 | 50526648 | stop gained | C/A;T | snv | 1 | ||||
rs11479 | 0.925 | 0.080 | 22 | 50525807 | stop gained | G/A;C;T | snv | 0.13; 1.3E-05; 4.3E-06 | 1 | ||
rs761665644 | 0.925 | 0.120 | 22 | 50527606 | missense variant | T/G | snv | 8.0E-06 | 4 | ||
rs74315511 | 0.925 | 0.240 | 22 | 50523994 | missense variant | C/T | snv | 8.0E-05 | 1.1E-04 | 4 | |
rs80358232 | 1.000 | 0.200 | 22 | 50523738 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
rs28937868 | 1.000 | 0.200 | 22 | 50524014 | missense variant | C/T | snv | 1 | |||
rs28937598 | 1.000 | 0.200 | 22 | 50523901 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs121913036 | 1.000 | 22 | 50526638 | missense variant | T/G | snv | 5.3E-05 | 4.9E-05 | 1 | ||
rs1064792867 | 1.000 | 22 | 50527611 | missense variant | A/C | snv | 1 | ||||
rs1064792873 | 1.000 | 22 | 50526141 | missense variant | C/T | snv | 1 | ||||
rs1064792874 | 1.000 | 22 | 50526019 | missense variant | C/T | snv | 1 | ||||
rs1060499532 | 1.000 | 22 | 50526338 | missense variant | A/G | snv | 1 | ||||
rs1064792869 | 1.000 | 22 | 50527215 | missense variant | C/T | snv | 1 | ||||
rs121913041 | 1.000 | 22 | 50527629 | missense variant | C/G;T | snv | 4.0E-06 | 1 | |||
rs946234163 | 1.000 | 22 | 50526639 | missense variant | C/T | snv | 7.0E-06 | 1 | |||
rs1060499533 | 1.000 | 22 | 50526293 | missense variant | A/G | snv | 1 | ||||
rs1064792870 | 1.000 | 22 | 50527170 | missense variant | T/G | snv | 7.0E-06 | 1 | |||
rs121913042 | 1.000 | 22 | 50526650 | missense variant | A/G | snv | 7.0E-06 | 1 | |||
rs764275775 | 1.000 | 22 | 50525859 | missense variant | C/A;G | snv | 1 | ||||
rs121913040 | 1.000 | 22 | 50526474 | missense variant | C/A;G;T | snv | 1.2E-05; 1.2E-05 | 1 | |||
rs121913039 | 1.000 | 22 | 50527612 | missense variant | C/T | snv | 3.3E-04 | 2.7E-04 | 1 |