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 | |||||
rs62160676 | 2 | 111410354 | intron variant | T/C;G | snv | 5 | |||||
rs218265 | 4 | 54542832 | intergenic variant | T/C | snv | 0.21 | 10 | ||||
rs7679673 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 28 | ||
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
rs7705526 | 0.776 | 0.240 | 5 | 1285859 | intron variant | C/A;T | snv | 15 | |||
rs2853961 | 6 | 31264212 | downstream gene variant | G/A | snv | 0.38 | 13 | ||||
rs6920211 | 6 | 135110180 | regulatory region variant | T/C | snv | 0.29 | 4 | ||||
rs4837892 | 9 | 121826025 | intron variant | G/T | snv | 0.36 | 13 | ||||
rs112505971 | 10 | 27068541 | intron variant | A/C;G | snv | 13 | |||||
rs334 | 0.724 | 0.240 | 11 | 5227002 | missense variant | T/A;C;G | snv | 3.5E-03 | 35 | ||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 41 | ||
rs7296503 | 12 | 41306962 | intron variant | C/T | snv | 0.57 | 13 | ||||
rs13331259 | 16 | 249924 | intron variant | A/G | snv | 3.0E-02 | 14 | ||||
rs3809627 | 16 | 30091839 | 5 prime UTR variant | C/A | snv | 0.41 | 5 | ||||
rs76792961 | 16 | 243594 | intron variant | C/T | snv | 7.3E-03 | 13 | ||||
rs3840870 | 17 | 50184820 | 3 prime UTR variant | -/CTTG | delins | 13 | |||||
rs17758695 | 18 | 63253621 | intron variant | C/T | snv | 2.1E-02 | 10 | ||||
rs78744187 | 19 | 33263642 | intergenic variant | C/T | snv | 6.8E-02 | 5 | ||||
rs1800961 | 0.851 | 0.160 | 20 | 44413724 | missense variant | C/T | snv | 3.1E-02 | 2.5E-02 | 21 | |
rs9917425 | 20 | 16755400 | intron variant | G/T | snv | 0.16 | 13 | ||||
rs8133974 | 21 | 35078544 | intron variant | C/T | snv | 0.11 | 3 |