Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 18 | |
rs855791 | 0.701 | 0.400 | 22 | 37066896 | missense variant | A/G;T | snv | 0.57; 4.0E-06 | 17 | ||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 16 | |
rs7776054 | 6 | 135097778 | intron variant | A/G | snv | 0.24 | 13 | ||||
rs7775698 | 1.000 | 0.080 | 6 | 135097497 | intron variant | C/T | snv | 6.9E-02 | 11 | ||
rs77542162 | 1.000 | 0.040 | 17 | 69085137 | missense variant | A/G | snv | 9.3E-03 | 1.0E-02 | 10 | |
rs17476364 | 10 | 69334748 | intron variant | T/C | snv | 6.4E-02 | 8 | ||||
rs144861591 | 6 | 26072764 | intergenic variant | C/T | snv | 3.8E-02 | 6 | ||||
rs147233090 | 0.925 | 0.040 | 15 | 43735849 | intron variant | C/T | snv | 1.7E-02 | 6 | ||
rs7385804 | 0.851 | 0.120 | 7 | 100638347 | intron variant | C/A | snv | 0.65 | 6 | ||
rs218237 | 4 | 54528005 | intergenic variant | C/T | snv | 0.18 | 5 | ||||
rs2413450 | 22 | 37074184 | intron variant | T/C | snv | 0.61 | 5 | ||||
rs62160676 | 2 | 111410354 | intron variant | T/C;G | snv | 5 | |||||
rs7955734 | 12 | 4223993 | intergenic variant | C/G | snv | 0.22 | 5 | ||||
rs9483788 | 6 | 135114363 | intergenic variant | T/C | snv | 0.19 | 3 | ||||
rs1331309 | 6 | 135085040 | intron variant | T/G | snv | 0.19 | 2 |