Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs36119840 | 0.807 | 0.280 | 5 | 37816010 | missense variant | G/A | snv | 2.3E-03 | 2.7E-03 | 3 | |
rs76262710 | 0.724 | 0.280 | 10 | 43113648 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs76397662 | 0.851 | 0.200 | 10 | 43102345 | missense variant | G/A | snv | 7.9E-04 | 2.9E-04 | 2 | |
rs8192466 | 1.000 | 0.120 | 11 | 27658560 | missense variant | G/A;T | snv | 1.3E-03; 1.6E-04 | 1 | ||
rs192489011 | 1.000 | 0.120 | 10 | 43100585 | missense variant | G/A;T | snv | 1.1E-03; 4.0E-06 | 1 | ||
rs552057730 | 1.000 | 0.120 | 10 | 43111238 | missense variant | C/A;T | snv | 8.0E-06; 1.6E-05 | 1 | ||
rs79658334 | 0.662 | 0.360 | 10 | 43119548 | missense variant | G/A;C;T | snv | 1.2E-04; 4.3E-06 | 1 | ||
rs79853121 | 1.000 | 0.120 | 10 | 43126651 | missense variant | C/A;T | snv | 3.6E-05 | 1 |