Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs967461896 | 0.724 | 0.240 | 17 | 7675086 | missense variant | A/C;G;T | snv | 16 | |||
rs942158624 | 0.724 | 0.320 | 17 | 7674948 | missense variant | T/A | snv | 16 | |||
rs886039484 | 0.641 | 0.440 | 17 | 7674888 | missense variant | T/C;G | snv | 10 | |||
rs876660821 | 0.689 | 0.400 | 17 | 7675075 | missense variant | A/C;G;T | snv | 21 | |||
rs876660807 | 0.763 | 0.160 | 17 | 7674248 | missense variant | T/C | snv | 12 | |||
rs876660754 | 0.701 | 0.360 | 17 | 7675095 | missense variant | C/A;T | snv | 18 | |||
rs876660333 | 0.742 | 0.360 | 17 | 7673805 | missense variant | A/C;G;T | snv | 13 | |||
rs876658468 | 0.689 | 0.440 | 17 | 7674954 | missense variant | G/A;C;T | snv | 22 | |||
rs867384286 | 0.732 | 0.240 | 4 | 152328233 | missense variant | G/A;C | snv | 4.3E-06 | 14 | ||
rs866987936 | 0.752 | 0.240 | 4 | 152326214 | missense variant | C/A;G;T | snv | 12 | |||
rs866775781 | 0.716 | 0.440 | 17 | 7675216 | splice acceptor variant | C/A;G | snv | 17 | |||
rs864622237 | 0.716 | 0.320 | 17 | 7674263 | missense variant | A/C;G;T | snv | 17 | |||
rs80338963 | 0.776 | 0.280 | 18 | 51065548 | missense variant | C/A;G;T | snv | 11 | |||
rs786203071 | 0.776 | 0.240 | 17 | 7675181 | missense variant | T/A;G | snv | 8 | |||
rs786202962 | 0.701 | 0.320 | 17 | 7675085 | missense variant | C/A;T | snv | 4.0E-06 | 17 | ||
rs786201838 | 0.683 | 0.440 | 17 | 7674953 | missense variant | T/A;C;G | snv | 23 | |||
rs786201419 | 0.790 | 0.160 | 17 | 7675180 | missense variant | C/A;T | snv | 8 | |||
rs786201059 | 0.701 | 0.360 | 17 | 7673764 | stop gained | C/A;G;T | snv | 19 | |||
rs786201057 | 0.677 | 0.400 | 17 | 7675995 | missense variant | G/A;C;T | snv | 24 | |||
rs765848205 | 0.763 | 0.240 | 17 | 7674253 | missense variant | A/C;G;T | snv | 12 | |||
rs764146326 | 0.662 | 0.480 | 17 | 7673779 | missense variant | C/A;G;T | snv | 4.0E-06 | 20 | ||
rs760043106 | 0.645 | 0.440 | 17 | 7674947 | missense variant | A/C;G;T | snv | 18 | |||
rs753660142 | 0.708 | 0.280 | 17 | 7673782 | missense variant | T/C;G | snv | 1.6E-05 | 19 | ||
rs747342068 | 0.695 | 0.440 | 17 | 7675218 | missense variant | T/C;G | snv | 4.0E-06 | 17 | ||
rs747241612 | 0.752 | 0.240 | 4 | 152326215 | missense variant | G/C | snv | 4.0E-06 | 12 |