Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs867538330 | 0.925 | 0.080 | 5 | 102458457 | synonymous variant | C/T | snv | 2 | |||
rs230490 | 0.882 | 0.080 | 4 | 102466262 | downstream gene variant | G/A | snv | 0.34 | 3 | ||
rs35767 | 0.763 | 0.360 | 12 | 102481791 | upstream gene variant | A/C;G;T | snv | 13 | |||
rs28362491 | 0.592 | 0.720 | 4 | 102500998 | non coding transcript exon variant | ATTG/- | delins | 56 | |||
rs28720239 | 1.000 | 0.080 | 4 | 102500998 | non coding transcript exon variant | ATTG/- | delins | 1 | |||
rs230510 | 1.000 | 0.080 | 4 | 102555009 | intron variant | T/A | snv | 0.37 | 1 | ||
rs3821958 | 1.000 | 0.080 | 4 | 102587667 | intron variant | A/G | snv | 0.42 | 1 | ||
rs3774959 | 0.925 | 0.080 | 4 | 102589957 | intron variant | G/A | snv | 0.34 | 2 | ||
rs3774964 | 1.000 | 0.080 | 4 | 102598330 | intron variant | A/G | snv | 0.39 | 1 | ||
rs997476 | 0.882 | 0.080 | 4 | 102620848 | downstream gene variant | G/T | snv | 4.3E-02 | 3 | ||
rs4450168 | 0.790 | 0.080 | 11 | 10265208 | intron variant | A/C;T | snv | 0.12 | 9 | ||
rs770635391 | 1.000 | 0.080 | 19 | 10271190 | missense variant | C/G;T | snv | 8.1E-06; 4.1E-06 | 1 | ||
rs750521832 | 0.732 | 0.200 | 11 | 102718452 | missense variant | A/G | snv | 4.0E-06 | 14 | ||
rs10883782 | 0.925 | 0.080 | 10 | 102824175 | intron variant | A/G | snv | 0.14 | 2 | ||
rs4919687 | 0.742 | 0.160 | 10 | 102835491 | non coding transcript exon variant | G/A | snv | 0.25 | 14 | ||
rs1799969 | 0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 | 38 | |
rs2094258 | 0.701 | 0.280 | 13 | 102844409 | intron variant | C/T | snv | 0.18 | 20 | ||
rs17724534 | 0.925 | 0.080 | 10 | 102845764 | non coding transcript exon variant | C/T | snv | 9.1E-02 | 2 | ||
rs751402 | 0.724 | 0.360 | 13 | 102845848 | 5 prime UTR variant | A/G | snv | 0.76 | 15 | ||
rs2296147 | 0.695 | 0.280 | 13 | 102846025 | 5 prime UTR variant | T/C | snv | 0.38 | 21 | ||
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 99 | |
rs2276109 | 0.701 | 0.440 | 11 | 102875061 | upstream gene variant | T/C | snv | 9.2E-02 | 18 | ||
rs17655 | 0.597 | 0.560 | 13 | 102875652 | missense variant | G/C | snv | 0.28 | 0.30 | 52 | |
rs873601 | 0.677 | 0.360 | 13 | 102875987 | 3 prime UTR variant | G/A | snv | 0.59 | 25 | ||
rs26802 | 0.925 | 0.160 | 3 | 10290681 | intron variant | T/G | snv | 0.31 | 3 |