Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs34682185 | 0.851 | 0.120 | 10 | 43106382 | missense variant | G/A | snv | 6.3E-04 | 2.2E-04 | 4 | |
rs377767391 | 0.827 | 0.160 | 10 | 43113627 | missense variant | T/A;C;G | snv | 2 | |||
rs377767394 | 0.925 | 0.080 | 10 | 43113603 | missense variant | A/C | snv | 2 | |||
rs377767395 | 0.882 | 0.120 | 10 | 43113613 | missense variant | A/G | snv | 4 | |||
rs377767397 | 0.790 | 0.280 | 10 | 43113628 | missense variant | G/A;C;T | snv | 7 | |||
rs377767398 | 0.807 | 0.280 | 10 | 43113628 | missense variant | GC/AT;CT;TT | mnv | 7 | |||
rs377767404 | 0.742 | 0.160 | 10 | 43114488 | missense variant | T/C | snv | 6 | |||
rs377767406 | 0.776 | 0.120 | 10 | 43114491 | missense variant | G/A;T | snv | 4.0E-05; 4.0E-06 | 8 | ||
rs377767414 | 0.925 | 0.080 | 10 | 43118397 | missense variant | G/A | snv | 2 | |||
rs377767415 | 0.925 | 0.120 | 10 | 43118418 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
rs377767426 | 1.000 | 0.080 | 10 | 43119694 | missense variant | C/G | snv | 1.8E-04 | 1.0E-04 | 2 | |
rs377767427 | 0.882 | 0.120 | 10 | 43120114 | missense variant | C/G | snv | 4.0E-06 | 3 | ||
rs377767429 | 0.790 | 0.120 | 10 | 43120120 | missense variant | GC/TT | mnv | 4 | |||
rs377767442 | 0.827 | 0.160 | 10 | 43121967 | missense variant | A/G | snv | 4 | |||
rs747844360 | 1.000 | 0.080 | 10 | 43112853 | missense variant | G/A | snv | 1.2E-05 | 1 | ||
rs74799832 | 0.662 | 0.280 | 10 | 43121968 | missense variant | T/C | snv | 4.0E-06 | 21 | ||
rs75030001 | 0.807 | 0.160 | 10 | 43118458 | missense variant | G/C;T | snv | 4.0E-06; 2.0E-05 | 4 | ||
rs750371239 | 1.000 | 0.080 | 11 | 108252912 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs75076352 | 0.689 | 0.240 | 10 | 43114500 | missense variant | T/A;C;G | snv | 1.2E-05 | 21 | ||
rs75234356 | 0.716 | 0.240 | 10 | 43120144 | missense variant | T/G | snv | 1.2E-05 | 7.0E-06 | 10 | |
rs75873440 | 0.763 | 0.200 | 10 | 43112173 | missense variant | G/A;T | snv | 4.4E-05 | 10 | ||
rs75996173 | 0.716 | 0.240 | 10 | 43114501 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 16 | ||
rs76262710 | 0.724 | 0.280 | 10 | 43113648 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06 | 11 | ||
rs769177037 | 1.000 | 0.080 | 1 | 161328467 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
rs770599902 | 1.000 | 0.080 | 1 | 161362382 | missense variant | G/A | snv | 4.0E-06 | 1 |