Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35388001 | 17 | 49779962 | intron variant | C/T | snv | 0.20 | 2 | ||||
rs79041579 | 17 | 49783553 | intron variant | G/A | snv | 0.15 | 2 | ||||
rs1123339 | 17 | 49789170 | non coding transcript exon variant | G/A | snv | 6.6E-02 | 2 | ||||
rs575705078 | 17 | 49779547 | intron variant | A/G | snv | 6.1E-04 | 1 |