Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs569108 | 0.790 | 0.200 | 11 | 60095631 | missense variant | A/G | snv | 4.7E-02 | 7.3E-02 | 8 | |
rs6967330 | 0.827 | 0.120 | 7 | 106018005 | missense variant | G/A | snv | 0.19 | 0.21 | 8 | |
rs2664538 | 0.827 | 0.200 | 20 | 46011586 | missense variant | A/G | snv | 6 | |||
rs11575936 | 0.851 | 0.200 | 6 | 137219288 | missense variant | C/T | snv | 1.3E-03 | 4.1E-04 | 4 | |
rs1805014 | 0.851 | 0.080 | 16 | 27363708 | missense variant | T/C | snv | 7.4E-03 | 1.4E-02 | 4 | |
rs1538660 | 0.882 | 0.080 | 9 | 108879545 | missense variant | G/A | snv | 0.19 | 0.22 | 3 | |
rs41347648 | 0.882 | 0.080 | 13 | 48707418 | missense variant | A/G | snv | 1.7E-02 | 1.7E-02 | 3 | |
rs55661460 | 0.882 | 0.120 | 5 | 159320326 | missense variant | C/T | snv | 2.2E-03 | 7.3E-04 | 3 | |
rs1362834154 | 0.925 | 0.080 | 16 | 27363681 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 2 | |
rs900333744 | 0.925 | 0.080 | 9 | 21440695 | missense variant | A/G | snv | 2 | |||
rs761019455 | 1.000 | 0.080 | 15 | 81299818 | missense variant | G/A | snv | 4.0E-05 | 2.8E-05 | 1 | |
rs1207011218 | 0.742 | 0.440 | 2 | 203870794 | synonymous variant | C/T | snv | 12 | |||
rs12603332 | 0.807 | 0.200 | 17 | 39926554 | 5 prime UTR variant | T/C | snv | 0.49 | 7 | ||
rs71802646 | 0.882 | 0.080 | 12 | 57111290 | 5 prime UTR variant | ACACACACACACACAC/-;AC;ACAC;ACACAC;ACACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACACAC;ACACACACACACACACACAC;ACACACACACACACACACACAC;ACACACACACACACACACACACAC;ACACACACACACACACACACACACAC | delins | 0.32 | 3 | ||
rs7081735 | 1.000 | 0.080 | 10 | 127998792 | 5 prime UTR variant | G/A | snv | 0.72 | 1 | ||
rs324015 | 0.827 | 0.120 | 12 | 57096317 | 3 prime UTR variant | T/C | snv | 0.76 | 5 | ||
rs4559 | 0.882 | 0.080 | 12 | 57095865 | 3 prime UTR variant | C/T | snv | 0.59 | 3 | ||
rs73985228 | 0.882 | 0.080 | 17 | 39922412 | 3 prime UTR variant | G/C;T | snv | 3 | |||
rs1425851607 | 0.925 | 0.080 | 9 | 21440691 | frameshift variant | C/- | delins | 4.2E-06 | 2 | ||
rs4950928 | 0.653 | 0.560 | 1 | 203186754 | upstream gene variant | G/A;C;T | snv | 33 | |||
rs7927894 | 0.742 | 0.320 | 11 | 76590272 | upstream gene variant | C/T | snv | 0.35 | 12 | ||
rs4794067 | 0.807 | 0.280 | 17 | 47731462 | upstream gene variant | T/A;C | snv | 0.25 | 7 | ||
rs928413 | 0.807 | 0.120 | 9 | 6213387 | upstream gene variant | G/A;C | snv | 7 | |||
rs10494132 | 0.851 | 0.080 | 1 | 111289601 | upstream gene variant | T/C | snv | 0.26 | 4 | ||
rs2233407 | 0.882 | 0.080 | 14 | 35405317 | upstream gene variant | T/A;C | snv | 3 |