Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2381416 | 1.000 | 0.080 | 9 | 6193455 | upstream gene variant | C/A | snv | 0.65 | 4 | ||
rs10455025 | 1.000 | 0.080 | 5 | 111069301 | upstream gene variant | A/C | snv | 0.24 | 3 | ||
rs16903574 | 0.882 | 0.120 | 5 | 14610200 | missense variant | C/A;G | snv | 4.0E-06; 5.6E-02 | 6 | ||
rs1837253 | 0.790 | 0.240 | 5 | 111066174 | upstream gene variant | T/C | snv | 0.72 | 10 | ||
rs2416257 | 0.882 | 0.160 | 5 | 111099792 | intron variant | C/G;T | snv | 5 | |||
rs4594881 | 1.000 | 0.080 | 5 | 35846713 | intergenic variant | G/T | snv | 0.28 | 2 | ||
rs1420101 | 0.827 | 0.280 | 2 | 102341256 | synonymous variant | C/T | snv | 0.33 | 0.35 | 8 | |
rs34290285 | 0.851 | 0.120 | 2 | 241759225 | intron variant | G/A | snv | 0.27 | 8 | ||
rs9807989 | 1.000 | 0.080 | 2 | 102354740 | intron variant | T/C;G | snv | 0.46 | 2 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
rs2814778 | 0.763 | 0.360 | 1 | 159204893 | 5 prime UTR variant | T/C | snv | 0.25 | 24 |