Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10487818 | 1.000 | 0.080 | 7 | 106269615 | intron variant | A/T | snv | 1.1E-02 | 1 | ||
rs1064891 | 0.925 | 0.080 | 10 | 6234611 | 3 prime UTR variant | T/C | snv | 0.37 | 2 | ||
rs121913564 | 0.882 | 0.080 | 18 | 60371403 | missense variant | A/C | snv | 2.0E-05 | 1.4E-05 | 3 | |
rs121913566 | 0.925 | 0.080 | 18 | 60372165 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs12510549 | 0.882 | 0.160 | 4 | 10274843 | intergenic variant | T/C | snv | 0.18 | 4 | ||
rs1322837244 | 0.925 | 0.080 | 19 | 45698622 | missense variant | C/T | snv | 2 | |||
rs13447331 | 0.925 | 0.080 | 18 | 60371970 | missense variant | G/A | snv | 1.7E-04 | 7.7E-05 | 2 | |
rs1799883 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 36 | ||
rs1800571 | 0.925 | 0.080 | 3 | 12381349 | missense variant | C/A | snv | 1.4E-05 | 2 | ||
rs1800949 | 1.000 | 0.080 | 6 | 131807424 | upstream gene variant | C/G;T | snv | 0.18 | 1 | ||
rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 131 | |
rs1805096 | 0.827 | 0.200 | 1 | 65636574 | synonymous variant | G/A | snv | 0.46 | 0.43 | 6 | |
rs1805097 | 0.689 | 0.360 | 13 | 109782884 | missense variant | C/G;T | snv | 0.35 | 22 | ||
rs1805134 | 0.925 | 0.160 | 1 | 65601426 | synonymous variant | T/C | snv | 0.22 | 0.24 | 2 | |
rs1805192 | 0.510 | 0.840 | 3 | 12379739 | missense variant | C/G | snv | 121 | |||
rs199951903 | 0.925 | 0.120 | MT | 15497 | missense variant | G/A | snv | 2 | |||
rs201408477 | 0.925 | 0.080 | 2 | 25161455 | missense variant | A/G | snv | 1.8E-04 | 1.6E-04 | 2 | |
rs2076349 | 0.882 | 0.120 | 1 | 209626885 | missense variant | C/T | snv | 0.13 | 0.13 | 3 | |
rs2229616 | 0.732 | 0.200 | 18 | 60372043 | missense variant | C/T | snv | 1.6E-02 | 1.6E-02 | 22 | |
rs2239607 | 0.925 | 0.120 | 12 | 109209475 | intron variant | A/G | snv | 0.14 | 3 | ||
rs2268388 | 0.851 | 0.200 | 12 | 109205840 | intron variant | G/A | snv | 0.14 | 6 | ||
rs28362491 | 0.592 | 0.720 | 4 | 102500998 | non coding transcript exon variant | ATTG/- | delins | 56 | |||
rs324420 | 0.637 | 0.440 | 1 | 46405089 | missense variant | C/A | snv | 0.24 | 0.26 | 48 | |
rs35859249 | 0.807 | 0.200 | 4 | 37902468 | missense variant | C/A;T | snv | 4.0E-06; 9.7E-02 | 6 | ||
rs3856806 | 0.637 | 0.440 | 3 | 12434058 | synonymous variant | C/T | snv | 0.13 | 0.11 | 41 |