Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs732774 | 0.827 | 0.320 | 13 | 51949672 | missense variant | C/T | snv | 0.57 | 0.56 | 5 | |
rs1061472 | 0.925 | 0.200 | 13 | 51950352 | missense variant | T/C;G | snv | 0.54 | 2 | ||
rs60986317 | 1.000 | 0.160 | 13 | 51934853 | missense variant | G/A | snv | 2.0E-03 | 2.8E-03 | 1 | |
rs72552259 | 1.000 | 0.160 | 13 | 51960274 | missense variant | C/T | snv | 1.5E-03; 4.0E-06 | 1.5E-03 | 1 | |
rs41292782 | 1.000 | 0.160 | 13 | 51946372 | missense variant | G/A | snv | 1.2E-03 | 1.5E-03 | 1 | |
rs181250704 | 1.000 | 0.160 | 13 | 51935019 | missense variant | G/A | snv | 1.1E-03 | 1.5E-03 | 1 | |
rs373762572 | 1.000 | 0.160 | 13 | 51974778 | missense variant | G/A;C | snv | 1.1E-03; 8.0E-06 | 1 | ||
rs76151636 | 0.776 | 0.280 | 13 | 51944145 | missense variant | G/A;T | snv | 4.0E-06; 9.2E-04 | 10 | ||
rs191312027 | 1.000 | 0.160 | 13 | 51950132 | stop gained | C/A;T | snv | 4.0E-06; 6.9E-04 | 1 | ||
rs121907998 | 1.000 | 0.160 | 13 | 51961849 | missense variant | A/C | snv | 5.2E-04 | 4.0E-04 | 1 | |
rs186924074 | 1.000 | 0.160 | 13 | 51961861 | missense variant | A/G | snv | 4.9E-04 | 5.8E-04 | 1 | |
rs200911496 | 1.000 | 0.160 | 13 | 51939062 | missense variant | T/C;G | snv | 3.2E-04; 4.0E-06 | 1 | ||
rs557577836 | 1.000 | 0.160 | 13 | 51974814 | missense variant | T/A;C | snv | 6.8E-05; 3.1E-04 | 1 | ||
rs201738967 | 1.000 | 0.160 | 13 | 51975098 | missense variant | T/C | snv | 2.4E-04 | 2.4E-04 | 1 | |
rs121907990 | 0.925 | 0.240 | 13 | 51937570 | missense variant | T/A;C | snv | 4.0E-06; 2.2E-04 | 2 | ||
rs199821556 | 1.000 | 0.160 | 13 | 51937493 | missense variant | C/T | snv | 2.0E-04 | 1.5E-04 | 1 | |
rs750019452 | 1.000 | 0.160 | 13 | 51949723 | missense variant | G/A | snv | 1.9E-04 | 3.5E-05 | 1 | |
rs572147914 | 1.000 | 0.160 | 13 | 51974407 | stop gained | G/A;T | snv | 1.9E-04; 9.7E-05 | 1 | ||
rs182659444 | 1.000 | 0.160 | 13 | 51942466 | missense variant | C/T | snv | 1.8E-04 | 4.9E-05 | 1 | |
rs374094065 | 1.000 | 0.160 | 13 | 51944161 | missense variant | T/G | snv | 1.5E-04 | 9.1E-05 | 1 | |
rs201061621 | 1.000 | 0.160 | 13 | 51946423 | missense variant | G/A;C;T | snv | 1.4E-04; 4.0E-06 | 1 | ||
rs28942074 | 0.851 | 0.240 | 13 | 51958333 | missense variant | C/A;T | snv | 1.4E-04; 3.2E-05 | 4 | ||
rs398123136 | 1.000 | 0.160 | 13 | 51958356 | synonymous variant | G/C | snv | 1.3E-04 | 4.9E-05 | 1 | |
rs753330854 | 1.000 | 0.160 | 13 | 51937332 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-04 | 1 | ||
rs541208827 | 1.000 | 0.160 | 13 | 51942482 | missense variant | C/T | snv | 1.2E-04 | 6.3E-05 | 1 |