Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9349205 | 6 | 41957421 | intron variant | G/A;C | snv | 6 | |||||
rs112233623 | 6 | 41957260 | intron variant | C/T | snv | 7.0E-03 | 5 | ||||
rs3218097 | 6 | 41937537 | intron variant | G/A;T | snv | 5 | |||||
rs9394841 | 6 | 41959197 | intron variant | T/C | snv | 0.22 | 3 | ||||
rs11970772 | 6 | 41957552 | intron variant | T/A | snv | 0.24 | 2 | ||||
rs16895130 | 6 | 41957193 | intron variant | A/G | snv | 0.22 | 2 | ||||
rs9296369 | 6 | 41953258 | intron variant | C/G;T | snv | 2 | |||||
rs9369327 | 6 | 42046566 | intron variant | C/T | snv | 6.5E-02 | 1 | ||||
rs9367125 | 6 | 42019806 | intron variant | G/C | snv | 0.10 | 1 | ||||
rs182679717 | 6 | 42007955 | intron variant | C/A;T | snv | 1 |