Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2000999 | 1.000 | 0.080 | 16 | 72074194 | intron variant | G/A | snv | 0.16 | 4 | ||
rs217181 | 16 | 72080103 | intron variant | C/T | snv | 0.20 | 2 | ||||
rs16973640 | 16 | 72050235 | intron variant | T/G | snv | 4.4E-02 | 1 | ||||
rs7191270 | 16 | 72051096 | intron variant | T/C | snv | 4.4E-02 | 1 |