Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs74956615 | 0.807 | 0.160 | 19 | 10317045 | 3 prime UTR variant | T/A;C | snv | 6 | |||
rs35018800 | 0.790 | 0.160 | 19 | 10354167 | missense variant | G/A | snv | 4.6E-03 | 4.9E-03 | 9 | |
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 12 | ||
rs280519 | 0.752 | 0.320 | 19 | 10362257 | splice region variant | A/C;G | snv | 0.50 | 10 | ||
rs2304256 | 0.732 | 0.360 | 19 | 10364976 | missense variant | C/A | snv | 0.27 | 0.23 | 13 | |
rs62131887 | 0.724 | 0.240 | 19 | 10476920 | intergenic variant | C/T | snv | 0.37 | 14 | ||
rs1239681664 | 0.716 | 0.320 | 9 | 104818690 | synonymous variant | A/G | snv | 7.0E-06 | 15 | ||
rs35074907 | 0.807 | 0.160 | 19 | 10489742 | synonymous variant | G/A | snv | 1.9E-02 | 1.5E-02 | 6 | |
rs2189234 | 1.000 | 0.040 | 4 | 105154341 | intron variant | T/G | snv | 0.62 | 3 | ||
rs10010325 | 1.000 | 0.040 | 4 | 105185196 | intron variant | C/A;G;T | snv | 4 | |||
rs11750385 | 0.827 | 0.120 | 5 | 10521556 | intron variant | G/A;T | snv | 5 | |||
rs7746082 | 0.851 | 0.160 | 6 | 105987394 | regulatory region variant | G/A;C | snv | 5 | |||
rs4946717 | 0.827 | 0.120 | 6 | 106026874 | intron variant | C/A;G;T | snv | 6 | |||
rs6911490 | 1.000 | 0.040 | 6 | 106074152 | intron variant | T/C | snv | 0.86 | 1 | ||
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 | 6 | ||
rs3776414 | 0.827 | 0.120 | 5 | 10689450 | intron variant | T/G | snv | 0.48 | 6 | ||
rs2930047 | 0.925 | 0.040 | 5 | 10695414 | intron variant | T/C | snv | 0.49 | 3 | ||
rs878859113 | 0.763 | 0.360 | 6 | 106971734 | missense variant | G/A | snv | 0.35 | 11 | ||
rs267939 | 1.000 | 0.040 | 5 | 10752203 | intron variant | C/T | snv | 0.50 | 1 | ||
rs11825977 | 0.925 | 0.040 | 11 | 1075920 | splice region variant | G/A | snv | 0.18 | 0.20 | 2 | |
rs17154444 | 1.000 | 0.040 | 7 | 107795423 | intron variant | T/C | snv | 4.8E-02 | 1 | ||
rs7805114 | 0.827 | 0.120 | 7 | 107809588 | downstream gene variant | T/A;G | snv | 5 | |||
rs2108225 | 1.000 | 0.040 | 7 | 107812658 | downstream gene variant | G/A;T | snv | 2 |