Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 5 | ||
rs4129267 | 0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv | 5 | |||
rs7529229 | 0.851 | 0.120 | 1 | 154448302 | intron variant | T/C | snv | 0.48 | 4 | ||
rs4537545 | 0.790 | 0.160 | 1 | 154446403 | intron variant | C/T | snv | 0.48 | 4 | ||
rs7518199 | 1 | 154434943 | intron variant | A/C;T | snv | 0.39; 4.2E-06 | 4 | ||||
rs4845625 | 0.851 | 0.080 | 1 | 154449591 | intron variant | T/C | snv | 0.60 | 3 | ||
rs12089132 | 1 | 154405860 | intron variant | T/C | snv | 1.2E-02 | 2 | ||||
rs1552481 | 1 | 154403877 | non coding transcript exon variant | C/T | snv | 0.94 | 2 | ||||
rs2229238 | 0.851 | 0.080 | 1 | 154465420 | 3 prime UTR variant | T/A;C | snv | 0.80 | 1 | ||
rs28638007 | 1 | 154448878 | intron variant | T/C | snv | 9.3E-02 | 1 | ||||
rs4845618 | 0.851 | 0.160 | 1 | 154427539 | intron variant | G/T | snv | 0.53 | 1 |