Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 35 | ||
rs1800961 | 0.851 | 0.160 | 20 | 44413724 | missense variant | C/T | snv | 3.1E-02 | 2.5E-02 | 17 | |
rs2074356 | 0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 | 9 | ||
rs2925979 | 1.000 | 0.080 | 16 | 81501185 | intron variant | T/A;C | snv | 9 | |||
rs12229654 | 0.763 | 0.320 | 12 | 110976657 | intergenic variant | T/G | snv | 4.8E-03 | 7 | ||
rs2972143 | 1.000 | 0.080 | 2 | 226251649 | intergenic variant | A/G | snv | 0.67 | 4 | ||
rs7185735 | 0.925 | 0.120 | 16 | 53788739 | intron variant | A/G;T | snv | 4 | |||
rs10734252 | 1.000 | 0.080 | 11 | 17383292 | non coding transcript exon variant | G/A | snv | 0.71 | 3 |