Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 5 | |||
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 | |||
rs80069458 | 0.882 | 0.120 | 10 | 43113629 | missense variant | C/G;T | snv | 2 | |||
rs121913233 | 0.627 | 0.520 | 11 | 533874 | missense variant | T/A;C;G | snv | 1 | |||
rs121913240 | 0.672 | 0.440 | 12 | 25227342 | missense variant | T/A;C;G | snv | 1 | |||
rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;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 | |||
rs377767432 | 0.925 | 0.160 | 10 | 43121980 | missense variant | C/A;T | snv | 1 | |||
rs55947360 | 1.000 | 0.120 | 10 | 43119669 | missense variant | G/A;T | snv | 4.0E-05; 4.0E-06 | 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 |