Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3764650 | 0.790 | 0.200 | 19 | 1046521 | intron variant | T/G | snv | 0.14 | 2 | ||
rs115550680 | 1.000 | 0.080 | 19 | 1050421 | intron variant | A/G | snv | 1.7E-02 | 1 | ||
rs3752246 | 1.000 | 0.080 | 19 | 1056493 | missense variant | G/C;T | snv | 0.84; 4.1E-06 | 1 | ||
rs4147929 | 0.882 | 0.120 | 19 | 1063444 | intron variant | A/C;G | snv | 1 |