Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9268402 | 0.827 | 0.200 | 6 | 32373576 | intron variant | G/A | snv | 0.45 | 4 | ||
rs6910071 | 0.790 | 0.320 | 6 | 32315077 | intron variant | A/G | snv | 0.14 | 3 | ||
rs9268403 | 0.807 | 0.240 | 6 | 32373696 | intron variant | T/C | snv | 0.24 | 3 | ||
rs9268145 | 0.925 | 0.160 | 6 | 32289507 | intron variant | T/G | snv | 0.14 | 2 | ||
rs9268362 | 0.925 | 0.160 | 6 | 32365564 | intron variant | A/G | snv | 0.16 | 0.15 | 2 | |
rs28366178 | 1.000 | 0.040 | 6 | 32308498 | intron variant | T/C | snv | 0.14 | 1 | ||
rs9268400 | 1.000 | 0.040 | 6 | 32372877 | intron variant | G/A | snv | 0.24 | 1 | ||
rs2281276 | 1.000 | 0.040 | 6 | 32372329 | intron variant | A/G | snv | 0.41 | 1 | ||
rs28361060 | 1.000 | 0.040 | 6 | 32336071 | intron variant | G/A | snv | 0.14 | 1 | ||
rs6913309 | 1.000 | 0.040 | 6 | 32372063 | intron variant | T/A | snv | 0.27 | 1 | ||
rs9268401 | 1.000 | 0.040 | 6 | 32373541 | intron variant | A/G | snv | 0.24 | 1 |