Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs872071 | 0.742 | 0.360 | 6 | 411064 | 3 prime UTR variant | A/G;T | snv | 13 | |||
rs735665 | 0.776 | 0.280 | 11 | 123490689 | intron variant | G/A | snv | 0.15 | 8 | ||
rs13397985 | 0.827 | 0.280 | 2 | 230226508 | intron variant | T/C;G | snv | 5 | |||
rs17483466 | 0.827 | 0.280 | 2 | 111039881 | intron variant | A/G | snv | 0.15 | 5 | ||
rs757978 | 0.851 | 0.200 | 2 | 241431686 | missense variant | C/A;T | snv | 4.1E-06; 9.3E-02 | 4 |