Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
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 | |||
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 | |||
rs387906629 | 0.925 | 0.080 | 3 | 128481270 | missense variant | G/A | snv | 1 | |||
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 | |||
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 | |||
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 | ||
rs1057519709 | 0.925 | 0.080 | 4 | 54733154 | missense variant | GA/AT | mnv | 1 | |||
rs121913514 | 0.763 | 0.240 | 4 | 54733174 | missense variant | T/A;G | snv | 1 | |||
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 1 | |
rs121913240 | 0.672 | 0.440 | 12 | 25227342 | missense variant | T/A;C;G | snv | 1 | |||
rs17851045 | 0.672 | 0.400 | 12 | 25227341 | missense variant | T/A;G | snv | 4.0E-06 | 1 | ||
rs111033563 | 0.776 | 0.240 | 6 | 26092916 | missense variant | A/C | snv | 4.0E-06 | 1 | ||
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 1 | |
rs104894226 | 0.658 | 0.560 | 11 | 534285 | missense variant | C/A;G;T | snv | 1 | |||
rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;G;T | snv | 1 |