Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11568373 | 2 | 168944893 | synonymous variant | T/C | snv | 5.8E-03 | 2.6E-02 | 3 | |||
rs16856314 | 2 | 168966582 | intron variant | G/A | snv | 3.0E-02 | 3 | ||||
rs2287623 | 2 | 168973645 | intron variant | G/A | snv | 0.57 | 1 | ||||
rs6709971 | 2 | 169011063 | intron variant | T/C | snv | 2.6E-02 | 3 |