Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 61 | ||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 25 | ||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 23 | |||||
rs334 | 0.724 | 0.240 | 11 | 5227002 | missense variant | T/A;C;G | snv | 3.5E-03 | 19 | ||
rs7705526 | 0.776 | 0.240 | 5 | 1285859 | intron variant | C/A;T | snv | 15 | |||
rs2519093 | 0.882 | 0.200 | 9 | 133266456 | intron variant | T/C | snv | 14 | |||
rs112505971 | 10 | 27068541 | intron variant | A/C;G | snv | 13 | |||||
rs3123543 | 1 | 212617344 | intron variant | T/A;C | snv | 13 | |||||
rs3840870 | 17 | 50184820 | 3 prime UTR variant | -/CTTG | delins | 13 | |||||
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 11 | |||||
rs140522 | 0.851 | 0.160 | 22 | 50532837 | upstream gene variant | T/A;C | snv | 10 | |||
rs550057 | 0.925 | 0.080 | 9 | 133271182 | intron variant | T/A;C | snv | 7 | |||
rs8887 | 1.000 | 0.080 | 19 | 4502189 | 3 prime UTR variant | T/C;G | snv | 0.51; 1.8E-05 | 6 | ||
rs9349205 | 6 | 41957421 | intron variant | G/A;C | snv | 6 | |||||
rs9472135 | 0.925 | 0.120 | 6 | 43842065 | intron variant | T/A;C;G | snv | 6 | |||
rs3218097 | 6 | 41937537 | intron variant | G/A;T | snv | 5 | |||||
rs4672497 | 2 | 62296430 | TF binding site variant | C/G;T | snv | 5 | |||||
rs4820268 | 0.851 | 0.160 | 22 | 37073551 | missense variant | G/A;C | snv | 0.53; 4.0E-06 | 5 | ||
rs62160676 | 2 | 111410354 | intron variant | T/C;G | snv | 5 | |||||
rs9804550 | 11 | 5164863 | intergenic variant | T/A;C | snv | 5 | |||||
rs113700287 | 3 | 24293020 | intron variant | -/GTT | delins | 4 | |||||
rs13335629 | 16 | 260381 | intron variant | G/A;C | snv | 1.1E-02 | 4 | ||||
rs150844304 | 15 | 43434427 | intron variant | A/C;G | snv | 4 |