Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11038167 | 1.000 | 0.040 | 11 | 44821583 | intron variant | A/C;G | snv | 1 | |||
rs11038172 | 1.000 | 0.040 | 11 | 44834046 | intron variant | A/G | snv | 5.1E-02 | 1 | ||
rs835784 | 1.000 | 0.040 | 11 | 44842267 | intron variant | A/G | snv | 0.52 | 1 |