Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387906661 | 0.807 | 0.280 | 7 | 140801551 | missense variant | T/G | snv | 2 | |||
rs121918456 | 0.752 | 0.280 | 12 | 112473023 | missense variant | A/C;G | snv | 2 | |||
rs397507549 | 0.742 | 0.240 | 12 | 112489104 | missense variant | C/A;G | snv | 2 | |||
rs80338796 | 0.667 | 0.480 | 3 | 12604200 | missense variant | G/A;C | snv | 4.0E-06 | 2 | ||
rs80338797 | 0.827 | 0.160 | 3 | 12584624 | missense variant | G/C;T | snv | 2 | |||
rs397507466 | 0.807 | 0.280 | 7 | 140801537 | missense variant | T/A;C;G | snv | 4.0E-06 | 1 | ||
rs587782343 | 0.851 | 0.200 | 10 | 87933073 | missense variant | G/A | snv | 1 | |||
rs587782360 | 0.851 | 0.280 | 10 | 87933162 | missense variant | A/G | snv | 1 | |||
rs121918457 | 0.701 | 0.280 | 12 | 112488466 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs121918468 | 0.882 | 0.160 | 12 | 112488444 | missense variant | G/A;T | snv | 1 | |||
rs121918469 | 0.882 | 0.160 | 12 | 112488454 | missense variant | G/C | snv | 1 | |||
rs121918470 | 0.790 | 0.160 | 12 | 112489105 | missense variant | A/C;G | snv | 4.0E-06 | 1 | ||
rs397507520 | 0.658 | 0.520 | 12 | 112453279 | missense variant | G/C;T | snv | 1 | |||
rs397507523 | 0.882 | 0.160 | 12 | 112472954 | missense variant | A/G | snv | 1 | |||
rs397507529 | 0.851 | 0.160 | 12 | 112473031 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
rs397507541 | 0.827 | 0.160 | 12 | 112489068 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs397507542 | 0.790 | 0.320 | 12 | 112489069 | missense variant | G/T | snv | 1 | |||
rs397509345 | 0.851 | 0.160 | 12 | 112489093 | missense variant | AG/CC | mnv | 1 | |||
rs80338798 | 0.925 | 0.160 | 3 | 12585761 | missense variant | C/T | snv | 1 | |||
rs80338799 | 0.882 | 0.160 | 3 | 12585745 | missense variant | G/A;C | snv | 1 |