Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4880 | 0.500 | 0.840 | 6 | 159692840 | missense variant | A/G | snv | 0.48 | 0.47 | 131 | |
rs4149584 | 0.683 | 0.440 | 12 | 6333477 | missense variant | C/G;T | snv | 4.0E-06; 1.3E-02 | 24 | ||
rs422951 | 0.807 | 0.280 | 6 | 32220606 | missense variant | T/C | snv | 0.40 | 0.40 | 8 | |
rs397514767 | 0.807 | 0.240 | 11 | 33710247 | missense variant | C/T | snv | 4.0E-06 | 7 | ||
rs1445335859 | 0.851 | 0.240 | X | 15331662 | missense variant | T/C | snv | 9.4E-06 | 5 |