Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3131296 | 0.807 | 0.320 | 6 | 32205216 | intron variant | C/T | snv | 0.11 | 6 | ||
rs7762279 | 0.807 | 0.360 | 6 | 32787513 | intergenic variant | T/C | snv | 8.4E-02 | 6 | ||
rs9272535 | 0.827 | 0.280 | 6 | 32638979 | synonymous variant | G/A | snv | 3.0E-05 | 1.8E-03 | 5 | |
rs9268856 | 0.807 | 0.240 | 6 | 32461942 | intron variant | C/A;T | snv | 4 | |||
rs9272219 | 0.925 | 0.160 | 6 | 32634492 | intron variant | G/T | snv | 0.29 | 4 | ||
rs3132935 | 0.925 | 0.160 | 6 | 32203298 | non coding transcript exon variant | A/G;T | snv | 2 | |||
rs9268862 | 0.925 | 0.160 | 6 | 32462390 | intron variant | A/C | snv | 0.29 | 2 |