Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12638862 | 0.827 | 0.160 | 3 | 169759718 | downstream gene variant | A/G | snv | 0.24 | 9 | ||
rs174548 | 0.851 | 0.160 | 11 | 61803876 | 5 prime UTR variant | C/G;T | snv | 9 | |||
rs2074356 | 0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 | 9 | ||
rs218265 | 4 | 54542832 | intergenic variant | T/C | snv | 0.21 | 9 | ||||
rs35979828 | 12 | 54292096 | intron variant | C/T | snv | 5.0E-02 | 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 | ||||
rs2283847 | 22 | 27785411 | intron variant | C/A;G;T | snv | 7 | |||||
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 | ||||
rs144861591 | 6 | 26072764 | intergenic variant | C/T | snv | 3.8E-02 | 6 | ||||
rs1505307 | 3 | 24301839 | intron variant | T/C | snv | 0.60 | 6 | ||||
rs17534202 | 1.000 | 0.120 | 1 | 203312047 | downstream gene variant | G/C | snv | 0.40 | 6 | ||
rs2853677 | 0.724 | 0.240 | 5 | 1287079 | 3 prime UTR variant | G/A | snv | 0.63 | 6 | ||
rs2979489 | 8 | 30423317 | intron variant | G/A;C | snv | 6 | |||||
rs4737010 | 8 | 41772929 | intron variant | G/A | snv | 0.32 | 6 | ||||
rs7203560 | 1.000 | 0.080 | 16 | 134391 | intron variant | T/G | snv | 2.0E-02 | 6 | ||
rs737092 | 20 | 57415349 | regulatory region variant | T/C | snv | 0.58 | 6 | ||||
rs7385804 | 0.851 | 0.120 | 7 | 100638347 | intron variant | C/A | snv | 0.65 | 6 | ||
rs8176746 | 0.882 | 0.160 | 9 | 133255935 | missense variant | G/A;T | snv | 4.1E-06; 0.12 | 6 | ||
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 | |||||
rs9399137 | 0.851 | 0.320 | 6 | 135097880 | intron variant | T/C | snv | 0.20 | 6 | ||
rs112233623 | 6 | 41957260 | intron variant | C/T | snv | 7.0E-03 | 5 |