Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5743810 | 0.689 | 0.360 | 4 | 38828729 | missense variant | A/G | snv | 0.73 | 0.72 | 21 | |
rs1051931 | 0.708 | 0.400 | 6 | 46705206 | missense variant | A/G | snv | 0.81 | 0.79 | 19 | |
rs3850641 | 0.716 | 0.400 | 1 | 173206693 | intron variant | A/G | snv | 0.14 | 17 | ||
rs72661131 | 0.742 | 0.480 | 10 | 52771739 | upstream gene variant | A/G | snv | 7.6E-04 | 15 | ||
rs867186 | 0.752 | 0.120 | 20 | 35176751 | missense variant | A/G | snv | 0.10 | 9.7E-02 | 15 | |
rs2227631 | 0.742 | 0.200 | 7 | 101126257 | upstream gene variant | A/G | snv | 0.54 | 13 | ||
rs20455 | 0.763 | 0.160 | 6 | 39357302 | missense variant | A/G | snv | 0.41 | 0.49 | 12 | |
rs762513613 | 0.752 | 0.280 | 1 | 161591315 | missense variant | A/G | snv | 4.2E-06 | 7.4E-06 | 11 | |
rs198389 | 0.776 | 0.240 | 1 | 11859214 | upstream gene variant | A/G | snv | 0.39 | 10 | ||
rs20551 | 0.752 | 0.320 | 22 | 41152004 | missense variant | A/G | snv | 0.31 | 0.23 | 10 | |
rs3825807 | 0.807 | 0.120 | 15 | 78796769 | missense variant | A/G | snv | 0.34 | 0.33 | 10 | |
rs6903956 | 0.763 | 0.160 | 6 | 11774350 | intron variant | A/G | snv | 0.65 | 10 | ||
rs2229116 | 0.827 | 0.080 | 15 | 33613209 | missense variant | A/G | snv | 0.23 | 0.21 | 9 | |
rs4523 | 0.776 | 0.280 | 19 | 3595796 | missense variant | A/G | snv | 0.56 | 0.66 | 8 | |
rs4773144 | 0.827 | 0.080 | 13 | 110308365 | intron variant | A/G | snv | 0.42 | 7 | ||
rs9370867 | 0.827 | 0.120 | 6 | 16145094 | missense variant | A/G | snv | 0.60 | 0.63 | 7 | |
rs879254840 | 0.827 | 0.120 | 19 | 11113322 | missense variant | A/G | snv | 5 | |||
rs1440763451 | 0.882 | 0.080 | 3 | 12416849 | missense variant | A/G | snv | 4.0E-06 | 4 | ||
rs4845623 | 0.925 | 0.040 | 1 | 154443301 | intron variant | A/G | snv | 0.47 | 4 | ||
rs4888378 | 0.851 | 0.040 | 16 | 75298143 | intron variant | A/G | snv | 0.52 | 4 | ||
rs201989364 | 0.882 | 0.080 | 3 | 186854295 | missense variant | A/G | snv | 6.4E-05 | 2.1E-05 | 3 | |
rs562020 | 1.000 | 0.040 | 13 | 33017932 | intron variant | A/G | snv | 0.69 | 1 | ||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs4673 | 0.653 | 0.600 | 16 | 88646828 | missense variant | A/G;T | snv | 0.70 | 32 | ||
rs2295490 | 0.724 | 0.320 | 20 | 388261 | missense variant | A/G;T | snv | 0.18; 4.0E-06 | 16 |