Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs2304256 | 0.732 | 0.360 | 19 | 10364976 | missense variant | C/A | snv | 0.27 | 0.23 | 13 | |
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 12 | ||
rs12720270 | 0.851 | 0.240 | 19 | 10365084 | intron variant | G/A | snv | 0.21 | 0.16 | 4 | |
rs280500 | 0.882 | 0.200 | 19 | 10379726 | 5 prime UTR variant | A/G | snv | 0.20 | 3 |