Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17465637 | 0.790 | 0.200 | 1 | 222650187 | intron variant | A/C;G;T | snv | 0.64; 6.4E-06 | 2 | ||
rs2133189 | 0.925 | 0.040 | 1 | 222641100 | intron variant | C/T | snv | 0.56 | 1 | ||
rs2291832 | 1.000 | 0.040 | 1 | 222653139 | intron variant | G/A;C | snv | 0.64; 1.2E-05 | 1 |