Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs193920774 | 0.695 | 0.440 | 17 | 7673823 | missense variant | C/A;T | snv | 22 | |||
rs121912654 | 0.683 | 0.400 | 17 | 7675143 | missense variant | C/A;T | snv | 4.0E-05 | 21 | ||
rs28934874 | 0.695 | 0.480 | 17 | 7675161 | missense variant | G/A;C;T | snv | 21 | |||
rs730882025 | 0.724 | 0.360 | 17 | 7674885 | missense variant | C/A;G;T | snv | 21 | |||
rs1057520002 | 0.695 | 0.360 | 17 | 7674242 | missense variant | A/C;G | snv | 20 | |||
rs730882005 | 0.701 | 0.400 | 17 | 7674250 | missense variant | C/A;G;T | snv | 8.0E-06 | 20 | ||
rs786201059 | 0.701 | 0.360 | 17 | 7673764 | stop gained | C/A;G;T | snv | 20 | |||
rs863224451 | 0.701 | 0.440 | 17 | 7673796 | missense variant | C/A;G;T | snv | 20 | |||
rs876660754 | 0.701 | 0.360 | 17 | 7675095 | missense variant | C/A;T | snv | 20 | |||
rs587780073 | 0.708 | 0.400 | 17 | 7674262 | missense variant | T/C;G | snv | 19 | |||
rs753660142 | 0.708 | 0.280 | 17 | 7673782 | missense variant | T/C;G | snv | 1.6E-05 | 19 | ||
rs148924904 | 0.724 | 0.360 | 17 | 7675124 | missense variant | T/C | snv | 7.0E-06 | 17 | ||
rs864622237 | 0.716 | 0.320 | 17 | 7674263 | missense variant | A/C;G;T | snv | 17 | |||
rs967461896 | 0.724 | 0.240 | 17 | 7675086 | missense variant | A/C;G;T | snv | 17 | |||
rs587781288 | 0.732 | 0.440 | 17 | 7675190 | missense variant | C/A;T | snv | 16 | |||
rs876659802 | 0.732 | 0.440 | 17 | 7673787 | missense variant | G/A;C;T | snv | 16 | |||
rs985033810 | 0.724 | 0.280 | 17 | 7674232 | missense variant | C/A;G;T | snv | 16 | |||
rs121912655 | 0.724 | 0.400 | 17 | 7674238 | missense variant | C/A;G;T | snv | 15 | |||
rs587782664 | 0.742 | 0.320 | 17 | 7674252 | missense variant | C/A;G;T | snv | 4.0E-06 | 15 | ||
rs730882026 | 0.742 | 0.440 | 17 | 7674256 | missense variant | T/C;G | snv | 15 | |||
rs587782177 | 0.763 | 0.200 | 17 | 7674887 | missense variant | C/A;G;T | snv | 11 | |||
rs1057519988 | 0.776 | 0.240 | 17 | 7673812 | missense variant | A/C;G;T | snv | 10 | |||
rs1057519995 | 0.807 | 0.240 | 17 | 7674200 | missense variant | T/A | snv | 9 | |||
rs1057519997 | 0.776 | 0.320 | 17 | 7676037 | missense variant | A/C;G;T | snv | 9 | |||
rs587782529 | 0.851 | 0.200 | 17 | 7670700 | missense variant | G/A;C | snv | 8 |