Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1952652 | 5 | 158384080 | intron variant | A/T | snv | 0.28 | 3 | ||||
rs10051330 | 5 | 158392616 | intron variant | A/G;T | snv | 2 | |||||
rs11960210 | 5 | 158390626 | intron variant | T/C;G | snv | 2 | |||||
rs12716337 | 5 | 158387220 | intron variant | T/A;C | snv | 2 | |||||
rs7701003 | 5 | 158397473 | intron variant | A/G | snv | 0.41 | 2 | ||||
rs9313772 | 5 | 158377449 | intron variant | C/T | snv | 0.30 | 2 | ||||
rs7719885 | 5 | 158389119 | intron variant | A/G | snv | 0.38 | 1 | ||||
rs2149954 | 0.882 | 0.080 | 5 | 158393594 | intron variant | C/T | snv | 0.37 | 5 |