Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 8 | ||
rs1883025 | 0.807 | 0.120 | 9 | 104902020 | intron variant | C/T | snv | 0.28 | 7 | ||
rs9515201 | 0.925 | 0.080 | 13 | 110388451 | intron variant | A/C | snv | 0.63 | 1 | ||
rs2074356 | 0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 | 12 | ||
rs2278426 | 1.000 | 0.080 | 19 | 11239812 | missense variant | C/T | snv | 0.11 | 0.11 | 2 | |
rs11102800 | 1.000 | 0.040 | 1 | 114498310 | intron variant | C/T | snv | 0.58 | 1 | ||
rs6701231 | 1 | 118953038 | intron variant | C/A;G | snv | 1 | |||||
rs984222 | 1 | 118961220 | intron variant | C/A;G | snv | 1 | |||||
rs6942652 | 7 | 121249218 | intron variant | G/C;T | snv | 1 | |||||
rs7776725 | 1.000 | 0.080 | 7 | 121393067 | intron variant | T/C | snv | 0.28 | 2 | ||
rs12110693 | 6 | 121837124 | intergenic variant | G/A | snv | 0.23 | 1 | ||||
rs10808546 | 8 | 125483576 | intron variant | C/T | snv | 0.39 | 4 | ||||
rs11154370 | 6 | 126846446 | intron variant | A/G;T | snv | 1 | |||||
rs987763 | 6 | 126960402 | intron variant | C/A;T | snv | 1 | |||||
rs1034207 | 6 | 127016554 | intron variant | C/A;G;T | snv | 0.94 | 1 | ||||
rs4580892 | 6 | 127088737 | intron variant | C/T | snv | 0.32 | 1 | ||||
rs9491696 | 6 | 127131494 | intron variant | C/G | snv | 0.45 | 1 | ||||
rs7745274 | 6 | 127188012 | intron variant | G/A | snv | 0.56 | 1 | ||||
rs620861 | 0.925 | 0.080 | 8 | 127323428 | intron variant | G/A | snv | 0.36 | 1 | ||
rs10894604 | 11 | 132771851 | non coding transcript exon variant | T/G | snv | 0.26 | 1 | ||||
rs645040 | 3 | 136207780 | upstream gene variant | G/T | snv | 0.77 | 1 | ||||
rs605066 | 6 | 139508529 | intron variant | C/T | snv | 0.53 | 4 | ||||
rs634869 | 6 | 139510620 | intron variant | T/A;C | snv | 2 | |||||
rs900400 | 0.925 | 0.080 | 3 | 157080986 | upstream gene variant | T/C | snv | 0.36 | 1 | ||
rs17213965 | 16 | 15788110 | intron variant | C/T | snv | 0.24 | 1 |