Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11112872 | 1.000 | 0.040 | 12 | 106111556 | intron variant | T/G | snv | 0.28 | 1 | ||
rs12449783 | 1.000 | 0.040 | 17 | 30200635 | intron variant | A/C;T | snv | 1 | |||
rs2297706 | 1.000 | 0.040 | 1 | 109914244 | intron variant | C/A;T | snv | 0.22 | 0.25 | 1 | |
rs333967 | 1.000 | 0.040 | 1 | 109917151 | intron variant | C/T | snv | 0.28 | 1 | ||
rs5906435 | 1.000 | 0.040 | X | 47589011 | intron variant | C/G;T | snv | 1 | |||
rs73318382 | 1.000 | 0.040 | 5 | 160467536 | intron variant | A/C | snv | 5.4E-02 | 1 | ||
rs7762544 | 0.882 | 0.040 | 6 | 41411577 | intergenic variant | G/A | snv | 0.81 | 3 | ||
rs1595009 | 1.000 | 0.040 | 4 | 73968939 | intergenic variant | C/T | snv | 0.61 | 1 | ||
rs1027009063 | 0.925 | 0.040 | 2 | 8802974 | stop gained | G/A | snv | 2 | |||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
rs1800470 | 0.515 | 0.840 | 19 | 41353016 | missense variant | G/A;C | snv | 0.55; 2.4E-04 | 107 | ||
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 99 | |
rs5743708 | 0.525 | 0.800 | 4 | 153705165 | missense variant | G/A | snv | 1.7E-02 | 1.8E-02 | 98 | |
rs763780 | 0.531 | 0.720 | 6 | 52236941 | missense variant | T/C | snv | 6.7E-02 | 6.6E-02 | 87 | |
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
rs61752717 | 0.583 | 0.840 | 16 | 3243407 | missense variant | T/A;C | snv | 2.8E-04 | 72 | ||
rs7041 | 0.576 | 0.800 | 4 | 71752617 | missense variant | A/C;T | snv | 0.52; 4.0E-06 | 64 | ||
rs1801275 | 0.581 | 0.680 | 16 | 27363079 | missense variant | A/G | snv | 0.25 | 0.36 | 58 | |
rs2066844 | 0.587 | 0.520 | 16 | 50712015 | missense variant | C/T | snv | 2.6E-02 | 2.9E-02 | 54 | |
rs4588 | 0.597 | 0.720 | 4 | 71752606 | missense variant | G/A;T | snv | 1.6E-05; 0.25 | 53 | ||
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 47 | |
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 46 | ||
rs148704956 | 0.716 | 0.360 | 6 | 52187772 | missense variant | A/G | snv | 8.0E-06 | 7.0E-06 | 19 |