Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1734907 | 0.925 | 0.080 | 7 | 100717894 | upstream gene variant | A/G | snv | 0.84 | 1 | ||
rs314313 | 1.000 | 0.040 | 7 | 100825743 | intron variant | T/A;C;G | snv | 0.29 | 2 | ||
rs503734 | 1.000 | 0.040 | 3 | 101304904 | intron variant | A/G | snv | 0.40 | 2 | ||
rs13126505 | 1.000 | 0.040 | 4 | 101944147 | intron variant | G/A | snv | 4.1E-02 | 3 | ||
rs13001325 | 1.000 | 0.040 | 2 | 102322576 | intron variant | C/T | snv | 0.30 | 2 | ||
rs1420098 | 2 | 102367819 | splice region variant | T/C | snv | 0.35 | 0.33 | 1 | |||
rs2058660 | 0.882 | 0.280 | 2 | 102437989 | intron variant | G/A | snv | 0.78 | 1 | ||
rs6708413 | 1.000 | 0.040 | 2 | 102446909 | intron variant | G/A | snv | 0.78 | 2 | ||
rs917997 | 0.701 | 0.480 | 2 | 102454108 | downstream gene variant | T/A;C | snv | 2 | |||
rs2274351 | 10 | 102504350 | intron variant | C/G;T | snv | 0.48 | 1 | ||||
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 2 | |
rs34536443 | 0.667 | 0.400 | 19 | 10352442 | missense variant | G/C | snv | 2.7E-02 | 2.8E-02 | 20 | |
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 | ||
rs11879191 | 1.000 | 0.040 | 19 | 10402235 | intron variant | G/A;C | snv | 2 | |||
rs35164067 | 1.000 | 0.040 | 19 | 10414505 | intron variant | G/A | snv | 0.18 | 2 | ||
rs2189234 | 1.000 | 0.040 | 4 | 105154341 | intron variant | T/G | snv | 0.62 | 3 | ||
rs6568421 | 1.000 | 0.040 | 6 | 105987150 | regulatory region variant | A/G | snv | 0.23 | 2 | ||
rs7746082 | 0.851 | 0.160 | 6 | 105987394 | regulatory region variant | G/A;C | snv | 3 | |||
rs4946717 | 0.827 | 0.120 | 6 | 106026874 | intron variant | C/A;G;T | snv | 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 | ||
rs4380874 | 1.000 | 0.040 | 7 | 107839870 | intergenic variant | T/A;C;G | snv | 2 | |||
rs11195128 | 1.000 | 0.040 | 10 | 110426390 | downstream gene variant | C/G;T | snv | 2 | |||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 61 |