Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121909210 | 0.708 | 0.200 | 5 | 136046406 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 15 | ||
rs121909715 | 0.790 | 0.160 | 9 | 121310819 | missense variant | G/A;T | snv | 4.0E-06 | 8 | ||
rs756465037 | 0.807 | 0.200 | 3 | 46439392 | missense variant | C/G | snv | 8.0E-06 | 7.0E-06 | 6 | |
rs267607109 | 0.827 | 0.160 | 5 | 136056754 | missense variant | C/A | snv | 5 | |||
rs267607110 | 0.851 | 0.160 | 5 | 136056769 | missense variant | C/A | snv | 4 |