Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13300663 | 9 | 4814948 | intron variant | G/A;C | snv | 3 | |||||
rs10974808 | 9 | 4840380 | intron variant | A/G | snv | 9.0E-02 | 2 | ||||
rs423955 | 9 | 4792339 | upstream gene variant | C/A;G;T | snv | 0.56 | 1 | ||||
rs457287 | 9 | 4834394 | intron variant | A/G;T | snv | 1 |