Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10505474 | 0.925 | 0.080 | 8 | 127405259 | intron variant | T/C | snv | 0.47 | 3 | ||
rs620861 | 0.925 | 0.080 | 8 | 127323428 | intron variant | G/A | snv | 0.36 | 3 | ||
rs16902104 | 1.000 | 0.080 | 8 | 127328663 | intron variant | C/G;T | snv | 1 | |||
rs7837328 | 0.882 | 0.120 | 8 | 127410882 | intron variant | A/G | snv | 0.52 | 8 | ||
rs7014346 | 0.732 | 0.240 | 8 | 127412547 | intron variant | A/G | snv | 0.63 | 14 | ||
rs13281615 | 0.716 | 0.360 | 8 | 127343372 | intron variant | A/G | snv | 0.43 | 18 | ||
rs10505477 | 0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 | 31 | ||
rs6983267 | 0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 | 62 |