Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11203203 | 0.807 | 0.240 | 21 | 42416077 | intron variant | G/A | snv | 0.28 | 5 | ||
rs12153855 | 0.776 | 0.320 | 6 | 32107027 | intron variant | T/C | snv | 0.11 | 10 | ||
rs12198173 | 0.827 | 0.240 | 6 | 32059031 | intron variant | G/A | snv | 0.10 | 9 | ||
rs1264350 | 0.925 | 0.160 | 6 | 30828768 | intron variant | T/C | snv | 9.4E-02 | 2 | ||
rs13199524 | 0.807 | 0.240 | 6 | 32098988 | intron variant | C/T | snv | 8.4E-02 | 8 | ||
rs1701704 | 0.851 | 0.200 | 12 | 56018703 | intron variant | T/G | snv | 0.25 | 5 | ||
rs2395185 | 0.724 | 0.360 | 6 | 32465390 | intron variant | G/T | snv | 0.29 | 8 | ||
rs3131296 | 0.807 | 0.320 | 6 | 32205216 | intron variant | C/T | snv | 0.11 | 6 | ||
rs3757247 | 0.827 | 0.320 | 6 | 90247744 | intron variant | C/T | snv | 0.38 | 2 | ||
rs3806156 | 0.827 | 0.280 | 6 | 32405921 | intron variant | G/A;T | snv | 5 | |||
rs2516049 | 0.742 | 0.400 | 6 | 32602623 | intergenic variant | T/C | snv | 0.27 | 9 | ||
rs2858870 | 0.851 | 0.280 | 6 | 32604474 | intergenic variant | T/A;C | snv | 2 | |||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
rs3132580 | 0.790 | 0.360 | 6 | 30952347 | missense variant | G/A | snv | 8.0E-02 | 9.3E-02 | 6 | |
rs3134942 | 0.790 | 0.320 | 6 | 32200994 | synonymous variant | G/T | snv | 9.7E-02 | 0.11 | 6 | |
rs3094061 | 0.925 | 0.160 | 6 | 30353412 | downstream gene variant | A/C;T | snv | 2 |