Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 24 | |||||
rs113918189 | 12 | 94325241 | intron variant | C/T | snv | 6.9E-02 | 2 | ||||
rs2984348 | X | 72308510 | intron variant | C/T | snv | 0.31 | 2 | ||||
rs35397826 | 17 | 68273941 | missense variant | A/G | snv | 0.12 | 0.11 | 2 | |||
rs7113624 | 11 | 87508051 | regulatory region variant | G/A;C | snv | 2 |