Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3859192 | 0.925 | 0.080 | 17 | 39972395 | intron variant | C/T | snv | 0.42 | 3 | ||
rs3894194 | 0.882 | 0.120 | 17 | 39965740 | missense variant | G/A | snv | 0.46 | 0.41 | 2 | |
rs3902025 | 0.925 | 0.080 | 17 | 39963001 | intron variant | G/T | snv | 0.56 | 2 | ||
rs6503526 | 0.925 | 0.080 | 17 | 39958345 | intron variant | C/T | snv | 0.41 | 2 | ||
rs1007654 | 1.000 | 0.080 | 17 | 39955101 | intron variant | A/G | snv | 0.69 | 1 | ||
rs7212938 | 0.925 | 0.120 | 17 | 39966427 | missense variant | G/A;C;T | snv | 4.1E-04; 4.2E-06; 0.52 | 1 | ||
rs7219080 | 1.000 | 0.080 | 17 | 39958263 | intron variant | A/C | snv | 0.65 | 1 |