Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs80358284 | 0.790 | 0.240 | 11 | 86952443 | missense variant | T/A;C | snv | 4.0E-06; 2.4E-05 | 10 | ||
rs878853243 | 0.851 | 0.160 | 7 | 120806619 | missense variant | C/A | snv | 4 | |||
rs28933684 | 0.882 | 0.160 | X | 43949831 | missense variant | G/A;T | snv | 3 | |||
rs104894874 | 0.882 | 0.160 | X | 43958521 | missense variant | T/C | snv | 5.5E-06 | 3 | ||
rs727504031 | 0.925 | 0.200 | X | 43949981 | missense variant | G/A | snv | 3 | |||
rs104894876 | 0.925 | 0.160 | X | 43949873 | missense variant | A/C | snv | 2 | |||
rs758550101 | 0.925 | 0.160 | X | 43958534 | missense variant | G/A;T | snv | 5.5E-06; 5.5E-06 | 2 | ||
rs104894878 | 0.925 | 0.160 | X | 43949840 | missense variant | G/A | snv | 2 | |||
rs1460859456 | 0.925 | 0.160 | X | 43950001 | missense variant | C/A;T | snv | 2 | |||
rs774200714 | 1.000 | 0.160 | 11 | 86954909 | missense variant | G/T | snv | 3.6E-05 | 5.6E-05 | 1 | |
rs104894870 | 1.000 | 0.160 | X | 43958515 | missense variant | T/C | snv | 1 | |||
rs104894872 | 1.000 | 0.160 | X | 43949995 | missense variant | C/G | snv | 1 | |||
rs104894873 | 1.000 | 0.160 | X | 43949817 | stop gained | G/A;T | snv | 3.1E-05 | 1 | ||
rs104894877 | 1.000 | 0.160 | X | 43949913 | missense variant | G/C | snv | 1 | |||
rs1057518793 | 1.000 | 0.160 | X | 43949933 | missense variant | G/A | snv | 1 | |||
rs137852221 | 1.000 | 0.160 | X | 43958512 | missense variant | A/T | snv | 1 | |||
rs104894867 | 1.000 | 0.160 | X | 43949932 | missense variant | C/A;G;T | snv | 1.2E-05; 2.4E-05 | 1 | ||
rs104894868 | 1.000 | 0.160 | X | 43949977 | missense variant | G/C | snv | 1 | |||
rs104894869 | 1.000 | 0.160 | X | 43950022 | missense variant | A/T | snv | 1 | |||
rs104894871 | 1.000 | 0.160 | X | 43949914 | missense variant | C/T | snv | 1 | |||
rs104894875 | 1.000 | 0.160 | X | 43949888 | missense variant | C/A;T | snv | 1 | |||
rs104894879 | 1.000 | 0.160 | X | 43958608 | missense variant | A/C | snv | 1 | |||
rs104894880 | 1.000 | 0.160 | X | 43950020 | missense variant | G/A | snv | 1 | |||
rs104894882 | 1.000 | 0.160 | X | 43949983 | stop gained | G/T | snv | 1 | |||
rs104894883 | 1.000 | 0.160 | X | 43949899 | missense variant | G/A | snv | 1 |