Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267606708 | 0.925 | 0.040 | 11 | 119278541 | missense variant | G/A | snv | 4.0E-06 | 2.1E-05 | 1 | |
rs28931590 | 1.000 | 0.040 | 19 | 33302164 | missense variant | T/A | snv | 1 | |||
rs869312828 | 0.807 | 0.080 | 5 | 177512369 | missense variant | C/T | snv | 1 | |||
rs147001633 | 0.776 | 0.240 | 2 | 25234373 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06; 2.2E-04 | 1 | ||
rs377577594 | 0.827 | 0.240 | 2 | 25234374 | missense variant | G/A;C;T | snv | 1.2E-04; 8.0E-06 | 1 | ||
rs137854451 | 0.925 | 0.080 | 19 | 856000 | missense variant | G/A | snv | 1 | |||
rs57246956 | 0.882 | 0.080 | 19 | 855649 | missense variant | G/A;T | snv | 1 | |||
rs121913487 | 0.925 | 0.120 | 13 | 28018503 | missense variant | A/C;T | snv | 2 | |||
rs121909646 | 0.882 | 0.120 | 13 | 28018504 | missense variant | T/A;G | snv | 1 | |||
rs121913232 | 0.925 | 0.120 | 13 | 28018500 | missense variant | G/C | snv | 1 | |||
rs121913488 | 0.807 | 0.120 | 13 | 28018505 | missense variant | C/A;G;T | snv | 1 | |||
rs387906631 | 0.882 | 0.080 | 3 | 128481901 | missense variant | G/A | snv | 2 | |||
rs387906629 | 0.925 | 0.080 | 3 | 128481270 | missense variant | G/A | snv | 1 | |||
rs104894230 | 0.564 | 0.600 | 11 | 534288 | missense variant | C/A;G;T | snv | 2 | |||
rs121913233 | 0.627 | 0.520 | 11 | 533874 | missense variant | T/A;C;G | snv | 1 | |||
rs121917759 | 0.790 | 0.480 | 11 | 533466 | missense variant | G/A | snv | 1 | |||
rs121913499 | 0.605 | 0.520 | 2 | 208248389 | missense variant | G/A;C;T | snv | 2 | |||
rs121913500 | 0.529 | 0.600 | 2 | 208248388 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 | ||
rs1057519906 | 0.882 | 0.120 | 15 | 90088607 | missense variant | T/A;C | snv | 1 | |||
rs121913502 | 0.708 | 0.320 | 15 | 90088702 | missense variant | C/A;T | snv | 3.2E-05 | 1 | ||
rs121913503 | 0.689 | 0.200 | 15 | 90088606 | missense variant | C/A;T | snv | 1 | |||
rs267606870 | 0.763 | 0.280 | 15 | 90088703 | missense variant | G/A;C | snv | 1 | |||
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 3 | ||
rs121912472 | 0.925 | 0.080 | 9 | 5073742 | missense variant | G/C | snv | 1 | |||
rs1127354 | 0.667 | 0.400 | 20 | 3213196 | missense variant | C/A;G | snv | 7.5E-02 | 1 |