Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121918459 | 0.662 | 0.440 | 12 | 112450368 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 47 | |
rs397507520 | 0.658 | 0.520 | 12 | 112453279 | missense variant | G/C;T | snv | 39 | |||
rs121918455 | 0.695 | 0.440 | 12 | 112477720 | missense variant | A/C;G | snv | 31 | |||
rs121918460 | 0.708 | 0.400 | 12 | 112450364 | missense variant | T/A;G | snv | 4.0E-06 | 27 | ||
rs121918457 | 0.701 | 0.280 | 12 | 112488466 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 24 | |
rs397507545 | 0.708 | 0.560 | 12 | 112489083 | missense variant | G/A;C | snv | 4.0E-06 | 20 | ||
rs121918453 | 0.732 | 0.280 | 12 | 112450394 | missense variant | G/A;C;T | snv | 19 | |||
rs397507531 | 0.752 | 0.320 | 12 | 112473040 | missense variant | T/C;G | snv | 18 | |||
rs121918454 | 0.742 | 0.280 | 12 | 112450395 | missense variant | C/A;G;T | snv | 17 | |||
rs28933386 | 0.752 | 0.400 | 12 | 112477719 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 15 | |
rs121918466 | 0.752 | 0.280 | 12 | 112450416 | missense variant | A/G | snv | 14 | |||
rs397507547 | 0.752 | 0.280 | 12 | 112489086 | missense variant | A/G | snv | 4.0E-06 | 14 | ||
rs121918456 | 0.752 | 0.280 | 12 | 112473023 | missense variant | A/C;G | snv | 13 | |||
rs121918462 | 0.742 | 0.320 | 12 | 112450398 | missense variant | C/T | snv | 13 | |||
rs397507549 | 0.742 | 0.240 | 12 | 112489104 | missense variant | C/A;G | snv | 13 | |||
rs121918470 | 0.790 | 0.160 | 12 | 112489105 | missense variant | A/C;G | snv | 4.0E-06 | 10 | ||
rs397507514 | 0.790 | 0.240 | 12 | 112450408 | missense variant | G/C;T | snv | 10 | |||
rs397507542 | 0.790 | 0.320 | 12 | 112489069 | missense variant | G/T | snv | 9 | |||
rs397507546 | 0.790 | 0.360 | 12 | 112489084 | missense variant | G/A;C;T | snv | 9 | |||
rs397507510 | 0.776 | 0.280 | 12 | 112450361 | missense variant | G/A;C;T | snv | 8 | |||
rs397507506 | 0.807 | 0.240 | 12 | 112450354 | missense variant | C/A;G | snv | 6 | |||
rs397507505 | 0.827 | 0.240 | 12 | 112450352 | missense variant | A/C;G;T | snv | 5 | |||
rs397507541 | 0.827 | 0.160 | 12 | 112489068 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 5 | |
rs397509345 | 0.851 | 0.160 | 12 | 112489093 | missense variant | AG/CC | mnv | 5 | |||
rs121918468 | 0.882 | 0.160 | 12 | 112488444 | missense variant | G/A;T | snv | 3 |