Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs4360494 | 0.776 | 0.080 | 1 | 37990219 | upstream gene variant | G/C | snv | 0.45 | 12 | ||
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 11 | |||||
rs738409 | 0.557 | 0.720 | 22 | 43928847 | missense variant | C/G | snv | 0.28 | 0.22 | 11 | |
rs7775698 | 1.000 | 0.080 | 6 | 135097497 | intron variant | C/T | snv | 6.9E-02 | 11 | ||
rs140522 | 0.851 | 0.160 | 22 | 50532837 | upstream gene variant | T/A;C | snv | 10 | |||
rs2277339 | 12 | 56752285 | missense variant | T/G | snv | 0.12 | 0.14 | 10 | |||
rs603424 | 1.000 | 0.080 | 10 | 100315722 | intron variant | G/A | snv | 0.34 | 10 | ||
rs715 | 1.000 | 0.040 | 2 | 210678331 | 3 prime UTR variant | T/C | snv | 0.28 | 10 | ||
rs76428106 | 0.851 | 0.040 | 13 | 28029870 | intron variant | T/C;G | snv | 10 | |||
rs77542162 | 1.000 | 0.040 | 17 | 69085137 | missense variant | A/G | snv | 9.3E-03 | 1.0E-02 | 10 | |
rs35979828 | 12 | 54292096 | intron variant | C/T | snv | 5.0E-02 | 9 | ||||
rs738408 | 0.925 | 0.120 | 22 | 43928850 | synonymous variant | C/T | snv | 0.28 | 0.22 | 9 | |
rs17476364 | 10 | 69334748 | intron variant | T/C | snv | 6.4E-02 | 8 | ||||
rs2075672 | 7 | 100642673 | intron variant | A/G | snv | 0.65 | 8 | ||||
rs9487023 | 6 | 109268801 | intron variant | A/G | snv | 0.40 | 8 | ||||
rs115849089 | 8 | 20054859 | intergenic variant | G/A | snv | 9.8E-02 | 7 | ||||
rs116843064 | 0.776 | 0.160 | 19 | 8364439 | missense variant | G/A | snv | 1.3E-02 | 1.5E-02 | 7 | |
rs3731211 | 9 | 21986848 | intron variant | T/A | snv | 0.74 | 7 | ||||
rs3747207 | 22 | 43928975 | intron variant | G/A | snv | 0.22 | 7 | ||||
rs4760 | 1.000 | 0.080 | 19 | 43648948 | missense variant | A/G | snv | 0.12 | 0.11 | 7 | |
rs863750 | 12 | 124020897 | intron variant | C/T | snv | 0.53 | 7 | ||||
rs1042034 | 0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 | 6 | |
rs1050828 | 0.790 | 0.200 | X | 154536002 | missense variant | C/T | snv | 9.1E-03 | 3.6E-02 | 6 | |
rs10758656 | 9 | 4852599 | intron variant | A/G | snv | 0.19 | 6 |