Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs377767429 | 0.790 | 0.120 | 10 | 43120120 | missense variant | GC/TT | mnv | 7 | |||
rs121913306 | 0.851 | 0.120 | 10 | 43120119 | missense variant | AGC/TTT | mnv | 4 | |||
rs74799832 | 0.662 | 0.280 | 10 | 43121968 | missense variant | T/C | snv | 4.0E-06 | 33 | ||
rs79658334 | 0.662 | 0.360 | 10 | 43119548 | missense variant | G/A;C;T | snv | 1.2E-04; 4.3E-06 | 29 | ||
rs75076352 | 0.689 | 0.240 | 10 | 43114500 | missense variant | T/A;C;G | snv | 1.2E-05 | 24 | ||
rs77939446 | 0.724 | 0.120 | 10 | 43113622 | missense variant | G/A;C;T | snv | 4.0E-06 | 15 | ||
rs377767406 | 0.776 | 0.120 | 10 | 43114491 | missense variant | G/A;T | snv | 4.0E-05; 4.0E-06 | 9 | ||
rs77558292 | 0.776 | 0.160 | 10 | 43113621 | missense variant | T/A;C;G | snv | 8 | |||
rs398122522 | 0.925 | 0.160 | 5 | 35070174 | missense variant | T/C | snv | 2 | |||
rs192767214 | 1.000 | 0.120 | 5 | 35065789 | missense variant | T/C | snv | 1 | |||
rs527783523 | 1.000 | 0.120 | 17 | 42299850 | missense variant | G/A | snv | 2.3E-04 | 7.0E-05 | 1 |