Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1122608 | 0.763 | 0.120 | 19 | 11052925 | intron variant | G/T | snv | 0.18 | 3 | ||
rs112374545 | 19 | 11078223 | intron variant | C/T | snv | 0.11 | 2 | ||||
rs12052201 | 19 | 11048420 | intron variant | G/T | snv | 0.17 | 2 | ||||
rs143020224 | 19 | 11076648 | intron variant | C/G;T | snv | 2 | |||||
rs17001095 | 19 | 11022596 | intron variant | A/G | snv | 0.33 | 2 | ||||
rs3786722 | 19 | 11050861 | intron variant | C/A | snv | 0.18 | 2 | ||||
rs73015011 | 19 | 11079088 | missense variant | T/C | snv | 0.13 | 2 | ||||
rs11669133 | 1.000 | 0.040 | 19 | 10981463 | intron variant | G/A | snv | 4.2E-02 | 1 |