Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13107612 | 0.827 | 0.120 | 4 | 101818823 | intron variant | C/T | snv | 0.31 | 5 | ||
rs4851529 | 0.827 | 0.120 | 2 | 102030838 | downstream gene variant | G/A | snv | 0.44 | 5 | ||
rs2310173 | 0.925 | 0.080 | 2 | 102047167 | intron variant | T/C;G | snv | 2 | |||
rs871656 | 0.827 | 0.120 | 2 | 102154822 | intron variant | T/A;C | snv | 5 | |||
rs12987977 | 0.827 | 0.120 | 2 | 102358876 | intron variant | T/G | snv | 0.31 | 5 | ||
rs2075184 | 0.724 | 0.240 | 2 | 102464132 | intergenic variant | T/C | snv | 0.78 | 14 | ||
rs3774937 | 0.776 | 0.280 | 4 | 102513096 | intron variant | T/C | snv | 0.26 | 5 | ||
rs74956615 | 0.807 | 0.160 | 19 | 10317045 | 3 prime UTR variant | T/A;C | snv | 5 | |||
rs35018800 | 0.790 | 0.160 | 19 | 10354167 | missense variant | G/A | snv | 4.6E-03 | 4.9E-03 | 5 | |
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 7 | ||
rs62131887 | 0.724 | 0.240 | 19 | 10476920 | intergenic variant | C/T | snv | 0.37 | 14 | ||
rs35074907 | 0.807 | 0.160 | 19 | 10489742 | synonymous variant | G/A | snv | 1.9E-02 | 1.5E-02 | 6 | |
rs11750385 | 0.827 | 0.120 | 5 | 10521556 | intron variant | G/A;T | snv | 5 | |||
rs4946717 | 0.827 | 0.120 | 6 | 106026874 | intron variant | C/A;G;T | snv | 6 | |||
rs28701841 | 0.827 | 0.120 | 6 | 106082455 | intron variant | G/A | snv | 7.6E-02 | 5 | ||
rs11839053 | 0.724 | 0.240 | 13 | 106410694 | intergenic variant | T/C | snv | 7.0E-02 | 14 | ||
rs12369214 | 0.807 | 0.120 | 12 | 106804833 | intron variant | G/A | snv | 0.41 | 5 | ||
rs3776414 | 0.827 | 0.120 | 5 | 10689450 | intron variant | T/G | snv | 0.48 | 6 | ||
rs7805114 | 0.827 | 0.120 | 7 | 107809588 | downstream gene variant | T/A;G | snv | 5 | |||
rs6466198 | 0.827 | 0.120 | 7 | 107839681 | regulatory region variant | A/T | snv | 0.68 | 5 | ||
rs7115956 | 0.827 | 0.120 | 11 | 110085620 | intron variant | C/T | snv | 0.38 | 5 | ||
rs4561177 | 0.807 | 0.120 | 11 | 110091706 | intron variant | A/G | snv | 0.36 | 6 | ||
rs8061882 | 0.827 | 0.120 | 16 | 11067551 | intron variant | G/C | snv | 0.11 | 5 | ||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 61 | ||
rs11649613 | 0.827 | 0.120 | 16 | 11225500 | downstream gene variant | C/T | snv | 0.37 | 5 |