Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11659570 | 18 | 49320739 | intron variant | C/T | snv | 0.31 | 1 | ||||
rs11664336 | 18 | 49078481 | intron variant | A/T | snv | 0.32 | 1 | ||||
rs117406288 | 18 | 49250518 | intron variant | C/T | snv | 1.1E-02 | 1 | ||||
rs12458127 | 18 | 49130988 | intron variant | C/T | snv | 0.10 | 1 | ||||
rs16950303 | 18 | 49055989 | intron variant | A/G | snv | 0.12 | 1 | ||||
rs1787200 | 18 | 49061284 | intron variant | G/A | snv | 0.71 | 1 | ||||
rs2878902 | 18 | 49124067 | intron variant | G/T | snv | 0.67 | 1 | ||||
rs71355378 | 18 | 49292340 | intron variant | A/G | snv | 3.8E-02 | 1 | ||||
rs9967417 | 18 | 49433130 | intron variant | G/C;T | snv | 1 |