Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs748409227 | 8 | 41708865 | synonymous variant | C/T | snv | 1.6E-05 | 7.0E-06 | 2 | |||
rs745525088 | 8 | 41714203 | missense variant | C/G;T | snv | 4.8E-06; 2.4E-05 | 1 | ||||
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
rs324420 | 0.637 | 0.440 | 1 | 46405089 | missense variant | C/A | snv | 0.24 | 0.26 | 48 | |
rs8065080 | 0.827 | 0.200 | 17 | 3577153 | missense variant | T/C | snv | 0.37 | 0.32 | 11 | |
rs920829 | 0.925 | 0.160 | 8 | 72065468 | missense variant | C/T | snv | 0.14 | 0.16 | 3 |