Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs1065852 | 0.695 | 0.360 | 22 | 42130692 | missense variant | G/A | snv | 0.21 | 0.19 | 19 | |
rs1135840 | 0.807 | 0.200 | 22 | 42126611 | missense variant | C/G | snv | 0.58 | 8 | ||
rs16947 | 0.882 | 0.040 | 22 | 42127941 | missense variant | G/A;T | snv | 5 | |||
rs1080985 | 0.925 | 0.080 | 22 | 42132375 | non coding transcript exon variant | G/A;C | snv | 2 |