Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3123543 | 1 | 212617344 | intron variant | T/A;C | snv | 13 | |||||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs6700896 | 0.827 | 0.160 | 1 | 65624099 | intron variant | C/T | snv | 0.44 | 9 | ||
rs17534202 | 1.000 | 0.120 | 1 | 203312047 | downstream gene variant | G/C | snv | 0.40 | 7 | ||
rs1434282 | 1 | 199041592 | non coding transcript exon variant | C/T | snv | 0.76 | 6 | ||||
rs1569419 | 1 | 3080038 | intron variant | T/C | snv | 0.73 | 5 | ||||
rs2492301 | 1 | 37473572 | intron variant | T/C | snv | 0.53 | 4 | ||||
rs61823972 | 1 | 205232197 | intron variant | A/C;T | snv | 4 | |||||
rs7529925 | 1 | 199038079 | intron variant | C/T | snv | 0.77 | 4 | ||||
rs2246434 | 1 | 158648665 | intron variant | G/A | snv | 0.26 | 0.22 | 3 | |||
rs10751450 | 1 | 203681817 | intron variant | C/G;T | snv | 2 | |||||
rs10923397 | 1 | 117708521 | regulatory region variant | C/T | snv | 0.14 | 2 | ||||
rs12135894 | 1 | 3811497 | downstream gene variant | C/A;T | snv | 2 | |||||
rs12563213 | 1 | 154318779 | upstream gene variant | G/C | snv | 0.30 | 2 | ||||
rs148046772 | 1 | 156314104 | intron variant | A/C;T | snv | 2 | |||||
rs1578741 | 1 | 117716081 | intergenic variant | A/C | snv | 0.19 | 2 | ||||
rs2340727 | 1 | 161976937 | intergenic variant | A/G | snv | 0.33 | 2 | ||||
rs34544423 | 1 | 198578103 | regulatory region variant | C/G | snv | 6.4E-02 | 2 | ||||
rs35229050 | 1 | 23514124 | intron variant | AA/-;A;AAA | delins | 0.53 | 2 | ||||
rs35340377 | 1 | 247874908 | intron variant | G/A | snv | 0.23 | 2 | ||||
rs3962382 | 1 | 67700010 | downstream gene variant | A/C;G | snv | 2 | |||||
rs4657616 | 1 | 159001296 | intron variant | A/G | snv | 0.31 | 2 | ||||
rs6540555 | 1 | 209763226 | intron variant | A/G | snv | 0.36 | 2 | ||||
rs826415 | 1 | 117611355 | intron variant | T/G | snv | 0.27 | 2 | ||||
rs11204538 | 1 | 247882970 | downstream gene variant | C/T | snv | 0.55 | 1 |