Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs77724903 | 0.672 | 0.280 | 10 | 43118460 | missense variant | A/G;T | snv | 4.0E-06; 2.1E-03 | 4 | ||
rs75076352 | 0.689 | 0.240 | 10 | 43114500 | missense variant | T/A;C;G | snv | 1.2E-05 | 3 | ||
rs75996173 | 0.716 | 0.240 | 10 | 43114501 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs76262710 | 0.724 | 0.280 | 10 | 43113648 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs77709286 | 0.752 | 0.160 | 10 | 43114502 | missense variant | C/G | snv | 4.0E-06 | 3 | ||
rs77939446 | 0.724 | 0.120 | 10 | 43113622 | missense variant | G/A;C;T | snv | 4.0E-06 | 3 | ||
rs79781594 | 0.732 | 0.160 | 10 | 43113649 | missense variant | G/A;C;T | snv | 3 | |||
rs377767391 | 0.827 | 0.160 | 10 | 43113627 | missense variant | T/A;C;G | snv | 2 | |||
rs377767405 | 0.827 | 0.120 | 10 | 43114489 | missense variant | G/A;C;T | snv | 2 | |||
rs74799832 | 0.662 | 0.280 | 10 | 43121968 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs75030001 | 0.807 | 0.160 | 10 | 43118458 | missense variant | G/C;T | snv | 4.0E-06; 2.0E-05 | 2 | ||
rs77316810 | 0.776 | 0.200 | 10 | 43113654 | missense variant | T/A;C;G | snv | 2 | |||
rs77503355 | 0.776 | 0.160 | 10 | 43113655 | missense variant | G/A;C;T | snv | 2 | |||
rs79890926 | 0.827 | 0.160 | 10 | 43113656 | missense variant | C/G;T | snv | 1.6E-05 | 2 | ||
rs80069458 | 0.882 | 0.120 | 10 | 43113629 | missense variant | C/G;T | snv | 2 | |||
rs121913308 | 0.827 | 0.120 | 10 | 43114492 | missense variant | A/C;G;T | snv | 1 | |||
rs377767397 | 0.790 | 0.280 | 10 | 43113628 | missense variant | G/A;C;T | snv | 1 | |||
rs377767429 | 0.790 | 0.120 | 10 | 43120120 | missense variant | GC/TT | mnv | 1 | |||
rs75234356 | 0.716 | 0.240 | 10 | 43120144 | missense variant | T/G | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs77558292 | 0.776 | 0.160 | 10 | 43113621 | missense variant | T/A;C;G | snv | 1 | |||
rs78014899 | 0.742 | 0.160 | 10 | 43118392 | missense variant | G/A;C;T | snv | 8.0E-06 | 1 | ||
rs78935588 | 1.000 | 0.120 | 10 | 43114519 | missense variant | C/G | snv | 1 | |||
rs79658334 | 0.662 | 0.360 | 10 | 43119548 | missense variant | G/A;C;T | snv | 1.2E-04; 4.3E-06 | 1 | ||
rs121908088 | 0.925 | 0.160 | 2 | 1494011 | stop gained | C/G;T | snv | 3.2E-04 | 1 |