Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 188 | |
rs1127354 | 0.667 | 0.400 | 20 | 3213196 | missense variant | C/A;G | snv | 7.5E-02 | 26 | ||
rs116855232 | 0.742 | 0.400 | 13 | 48045719 | missense variant | C/T | snv | 2.8E-02 | 1.1E-02 | 12 | |
rs2228391 | 0.882 | 0.160 | 6 | 32829996 | missense variant | T/C | snv | 1.3E-02 | 3.9E-03 | 3 | |
rs185386680 | 0.925 | 0.040 | 6 | 31207153 | downstream gene variant | A/G | snv | 1.2E-03 | 2 | ||
rs1736557 | 0.925 | 0.160 | 1 | 171110939 | missense variant | G/A | snv | 8.2E-02 | 6.3E-02 | 2 | |
rs114291795 | 0.925 | 0.040 | 6 | 31409863 | intron variant | C/G | snv | 3.0E-02 | 2 | ||
rs2596487 | 1.000 | 0.040 | 6 | 31357279 | non coding transcript exon variant | C/T | snv | 0.31 | 1 |