Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 | ||
rs1167827 | 7 | 75533848 | 3 prime UTR variant | G/A | snv | 0.37 | 5 | ||||
rs17151637 | 8 | 10295572 | intron variant | C/G;T | snv | 2 | |||||
rs4354968 | 16 | 76434236 | intron variant | T/A;C | snv | 2 |