Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2715555 | 0.925 | 0.080 | 17 | 40388372 | downstream gene variant | G/A | snv | 9.5E-02 | 2 | ||
rs3217304 | 0.925 | 0.080 | 2 | 98544046 | intron variant | ACACAC/-;AC;ACAC;ACACACAC;ACACACACAC;ACACACACACAC | delins | 0.25 | 2 | ||
rs3776944 | 0.925 | 0.080 | 5 | 179793009 | upstream gene variant | G/A | snv | 8.4E-02 | 2 | ||
rs3806448 | 0.925 | 0.080 | 1 | 111289583 | upstream gene variant | G/A | snv | 0.45 | 2 | ||
rs533116 | 0.925 | 0.120 | 11 | 60860110 | upstream gene variant | C/T | snv | 0.28 | 2 | ||
rs900333744 | 0.925 | 0.080 | 9 | 21440695 | missense variant | A/G | snv | 2 | |||
rs7081735 | 1.000 | 0.080 | 10 | 127998792 | 5 prime UTR variant | G/A | snv | 0.72 | 1 | ||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs1425851607 | 0.925 | 0.080 | 9 | 21440691 | frameshift variant | C/- | delins | 4.2E-06 | 2 | ||
rs61816761 | 0.658 | 0.640 | 1 | 152313385 | stop gained | G/A;T | snv | 9.4E-03; 8.0E-06 | 43 | ||
rs1362834154 | 0.925 | 0.080 | 16 | 27363681 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 2 | |
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 57 | ||
rs555743307 | 0.695 | 0.440 | 16 | 27342243 | missense variant | G/A;T | snv | 3.6E-05; 2.9E-04 | 20 | ||
rs761019455 | 1.000 | 0.080 | 15 | 81299818 | missense variant | G/A | snv | 4.0E-05 | 2.8E-05 | 1 | |
rs11575936 | 0.851 | 0.200 | 6 | 137219288 | missense variant | C/T | snv | 1.3E-03 | 4.1E-04 | 4 | |
rs55661460 | 0.882 | 0.120 | 5 | 159320326 | missense variant | C/T | snv | 2.2E-03 | 7.3E-04 | 3 | |
rs1805014 | 0.851 | 0.080 | 16 | 27363708 | missense variant | T/C | snv | 7.4E-03 | 1.4E-02 | 4 | |
rs41347648 | 0.882 | 0.080 | 13 | 48707418 | missense variant | A/G | snv | 1.7E-02 | 1.7E-02 | 3 | |
rs569108 | 0.790 | 0.200 | 11 | 60095631 | missense variant | A/G | snv | 4.7E-02 | 7.3E-02 | 8 | |
rs3135932 | 0.677 | 0.480 | 11 | 117993348 | missense variant | A/G | snv | 0.13 | 0.11 | 23 | |
rs11650354 | 1.000 | 0.080 | 17 | 47744726 | intron variant | C/A;T | snv | 0.16 | 0.15 | 1 | |
rs17577 | 0.649 | 0.520 | 20 | 46014472 | missense variant | G/A;C | snv | 0.16 | 31 | ||
rs6967330 | 0.827 | 0.120 | 7 | 106018005 | missense variant | G/A | snv | 0.19 | 0.21 | 8 | |
rs1538660 | 0.882 | 0.080 | 9 | 108879545 | missense variant | G/A | snv | 0.19 | 0.22 | 3 | |
rs9808753 | 0.701 | 0.400 | 21 | 33415005 | missense variant | A/G | snv | 0.20 | 0.18 | 17 |