Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs58072617 | 0.790 | 0.120 | 12 | 52517702 | missense variant | A/G;T | snv | 7 | |||
rs60399023 | 0.827 | 0.200 | 17 | 41586462 | missense variant | G/A;C | snv | 5 | |||
rs58330629 | 0.851 | 0.120 | 17 | 41586461 | missense variant | C/A;G;T | snv | 4 | |||
rs59190510 | 0.851 | 0.080 | 12 | 52516647 | stop gained | C/A;T | snv | 4 | |||
rs28928893 | 0.882 | 0.120 | 17 | 41586479 | missense variant | A/G | snv | 3 | |||
rs58762773 | 0.882 | 0.080 | 17 | 41583245 | missense variant | C/G;T | snv | 4.0E-06 | 3 | ||
rs60586163 | 0.882 | 0.080 | 12 | 52519137 | missense variant | G/A;C;T | snv | 4.0E-06 | 3 | ||
rs58380626 | 0.925 | 0.080 | 17 | 41583266 | missense variant | A/G | snv | 2 | |||
rs59110575 | 0.925 | 0.080 | 17 | 41586471 | missense variant | G/A | snv | 2 | |||
rs60171927 | 0.925 | 0.080 | 17 | 41586467 | missense variant | T/C | snv | 2 | |||
rs60470268 | 0.925 | 0.080 | 17 | 41586450 | missense variant | A/C | snv | 2 | |||
rs60715293 | 0.925 | 0.080 | 12 | 52519756 | missense variant | A/G | snv | 2 | |||
rs61348633 | 0.925 | 0.080 | 12 | 52516652 | missense variant | T/C | snv | 2 | |||
rs3826549 | 1.000 | 0.080 | 17 | 41586466 | missense variant | A/G;T | snv | 0.64 | 1 | ||
rs57364972 | 1.000 | 0.080 | 17 | 41583253 | missense variant | A/T | snv | 1 | |||
rs57522245 | 1.000 | 0.080 | 17 | 41586446 | missense variant | A/G | snv | 1 | |||
rs60622724 | 1.000 | 0.080 | 17 | 41583262 | missense variant | C/A;G;T | snv | 4.0E-06; 6.0E-05 | 1 | ||
rs60993843 | 1.000 | 0.080 | 17 | 41586476 | missense variant | T/C;G | snv | 1 | |||
rs61085704 | 1.000 | 0.080 | 17 | 41583259 | missense variant | C/A;G;T | snv | 4.0E-06; 4.4E-05 | 1 | ||
rs267607456 | 1.000 | 0.080 | 12 | 52519802 | missense variant | C/A;G | snv | 1 | |||
rs57155193 | 1.000 | 0.080 | 12 | 52516653 | missense variant | C/T | snv | 1 | |||
rs57781042 | 1.000 | 0.080 | 12 | 52519761 | missense variant | A/G | snv | 1 | |||
rs57890479 | 1.000 | 0.080 | 12 | 52519774 | missense variant | G/A | snv | 1 | |||
rs58619430 | 1.000 | 0.080 | 12 | 52519795 | missense variant | C/T | snv | 1 | |||
rs59092197 | 1.000 | 0.080 | 12 | 52519770 | missense variant | T/C | snv | 1 |