Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6918289 | 0.925 | 0.040 | 6 | 41134089 | intron variant | G/T | snv | 9.8E-02 | 2 | ||
rs7177922 | 0.925 | 0.040 | 15 | 33616418 | intron variant | G/A | snv | 0.19 | 2 | ||
rs749582333 | 0.925 | 0.040 | 11 | 89340157 | frameshift variant | G/- | delins | 2 | |||
rs750996166 | 0.925 | 0.040 | 1 | 161041409 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 2 | |
rs767523236 | 0.925 | 0.040 | 17 | 58279033 | missense variant | T/C | snv | 4.1E-06 | 7.0E-06 | 2 | |
rs769442590 | 0.925 | 0.040 | 8 | 19960927 | missense variant | A/C;G | snv | 1.6E-05 | 2 | ||
rs915014 | 0.925 | 0.040 | 1 | 11789412 | missense variant | T/C | snv | 2 | |||
rs10276782 | 1.000 | 0.040 | 7 | 24765621 | regulatory region variant | C/T | snv | 0.13 | 1 | ||
rs11781551 | 1.000 | 0.040 | 8 | 122395852 | intergenic variant | G/A | snv | 0.40 | 1 | ||
rs17045031 | 1.000 | 0.040 | 3 | 66717940 | intergenic variant | G/A | snv | 0.10 | 1 | ||
rs562020 | 1.000 | 0.040 | 13 | 33017932 | intron variant | A/G | snv | 0.69 | 1 | ||
rs567170 | 1.000 | 0.040 | 13 | 33043649 | intron variant | C/G | snv | 0.32 | 1 | ||
rs6601530 | 1.000 | 0.040 | 8 | 10813762 | intron variant | G/A | snv | 0.61 | 1 | ||
rs747885829 | 1.000 | 0.040 | 1 | 247423957 | missense variant | C/T | snv | 2.0E-05 | 1.4E-05 | 1 | |
rs445925 | 0.882 | 0.080 | 19 | 44912383 | non coding transcript exon variant | G/A;C | snv | 10 | |||
rs1866389 | 0.790 | 0.080 | 5 | 80065442 | missense variant | G/C | snv | 0.17 | 0.17 | 9 | |
rs2229116 | 0.827 | 0.080 | 15 | 33613209 | missense variant | A/G | snv | 0.23 | 0.21 | 9 | |
rs67608943 | 0.851 | 0.080 | 1 | 55046549 | stop gained | C/G;T | snv | 1.9E-04 | 8 | ||
rs4773144 | 0.827 | 0.080 | 13 | 110308365 | intron variant | A/G | snv | 0.42 | 7 | ||
rs2453021 | 0.807 | 0.080 | 1 | 7929506 | intron variant | C/A;T | snv | 6 | |||
rs28362286 | 0.851 | 0.080 | 1 | 55063542 | stop gained | C/A;T | snv | 5.6E-04 | 6 | ||
rs7439293 | 0.807 | 0.080 | 4 | 168756335 | non coding transcript exon variant | G/A | snv | 0.44 | 6 | ||
rs974819 | 0.807 | 0.080 | 11 | 103789839 | intron variant | T/A;C | snv | 6 | |||
rs2229238 | 0.851 | 0.080 | 1 | 154465420 | 3 prime UTR variant | T/A;C | snv | 0.80 | 5 | ||
rs4076317 | 0.882 | 0.080 | 19 | 8364115 | intron variant | C/G | snv | 0.25 | 5 |