Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12170597 | 1.000 | 22 | 46534853 | missense variant | G/A | snv | 1.2E-03 | 5.2E-03 | 1 | ||
rs199688538 | 1.000 | 22 | 46378661 | missense variant | C/T | snv | 4.8E-04 | 4.3E-04 | 1 | ||
rs6008777 | 1.000 | 22 | 46364140 | missense variant | G/A | snv | 5.9E-03 | 2.6E-02 | 1 | ||
rs61741871 | 1.000 | 22 | 46364084 | missense variant | G/C | snv | 7.9E-03 | 3.2E-02 | 1 | ||
rs778976254 | 1.000 | 14 | 58638335 | missense variant | C/T | snv | 6.0E-04 | 2.1E-05 | 1 | ||
rs1114167354 | 1.000 | 10 | 34341696 | missense variant | T/C | snv | 1 | ||||
rs199923448 | 1.000 | 10 | 34382893 | missense variant | C/A;T | snv | 8.0E-06; 5.6E-05 | 1 | |||
rs781461462 | 1.000 | 10 | 34331221 | missense variant | G/A;C;T | snv | 1.6E-05 | 1 | |||
rs1302482009 | 1.000 | 8 | 143810730 | missense variant | G/A | snv | 2.8E-05 | 1 | |||
rs782428100 | 1.000 | 8 | 143792044 | missense variant | C/T | snv | 5.2E-05 | 9.1E-05 | 1 | ||
rs121918219 | 1.000 | 1 | 115682372 | missense variant | G/A | snv | 2.4E-05 | 4.2E-05 | 1 | ||
rs121918220 | 1.000 | 1 | 115683980 | missense variant | T/C | snv | 1.2E-05 | 7.0E-06 | 1 | ||
rs146695372 | 1.000 | 1 | 115663704 | missense variant | C/T | snv | 6.0E-05 | 9.8E-05 | 1 | ||
rs761123443 | 1.000 | 1 | 115663998 | missense variant | G/A | snv | 2.4E-05 | 6.3E-05 | 1 | ||
rs775571796 | 1.000 | 1 | 115685423 | missense variant | G/T | snv | 1.2E-05 | 1 | |||
rs267607167 | 1.000 | 1 | 160421171 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 1 | |||
rs267607168 | 1.000 | 1 | 160425122 | missense variant | T/C | snv | 1 |