Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2228612 | 0.763 | 0.160 | 19 | 10162696 | missense variant | T/A;C;G | snv | 0.14 | 12 | ||
rs1284806277 | 0.827 | 0.200 | 14 | 102251978 | missense variant | A/G | snv | 1.4E-05 | 13 | ||
rs230490 | 0.882 | 0.080 | 4 | 102466262 | downstream gene variant | G/A | snv | 0.34 | 3 | ||
rs4648110 | 0.925 | 0.080 | 4 | 102612664 | intron variant | T/A | snv | 0.22 | 3 | ||
rs997476 | 0.882 | 0.080 | 4 | 102620848 | downstream gene variant | G/T | snv | 4.3E-02 | 3 | ||
rs750521832 | 0.732 | 0.200 | 11 | 102718452 | missense variant | A/G | snv | 4.0E-06 | 14 | ||
rs7911488 | 0.882 | 0.080 | 10 | 103394332 | 5 prime UTR variant | A/G | snv | 0.34 | 0.26 | 3 | |
rs4135113 | 0.925 | 0.080 | 12 | 103982915 | missense variant | G/A;C;T | snv | 4.7E-02 | 5 | ||
rs2302615 | 0.807 | 0.120 | 2 | 10448012 | intron variant | C/T | snv | 0.31 | 7 | ||
rs1383147053 | 0.882 | 0.120 | 7 | 107901762 | missense variant | G/A | snv | 4 | |||
rs1805097 | 0.689 | 0.360 | 13 | 109782884 | missense variant | C/G;T | snv | 0.35 | 22 | ||
rs773442580 | 0.851 | 0.080 | 4 | 109913367 | missense variant | T/C;G | snv | 4.0E-06 | 7 | ||
rs3802842 | 0.695 | 0.280 | 11 | 111300984 | intron variant | C/A | snv | 0.71 | 25 | ||
rs777980327 | 0.716 | 0.280 | 5 | 112837567 | missense variant | A/T | snv | 4.0E-06 | 7.0E-06 | 21 | |
rs1380087059 | 0.882 | 0.160 | 5 | 112837749 | missense variant | G/C | snv | 4.0E-06 | 3 | ||
rs587781394 | 0.882 | 0.160 | 5 | 112837812 | missense variant | G/A;C | snv | 4.0E-06; 8.0E-06 | 3 | ||
rs1463038513 | 0.658 | 0.440 | 5 | 112839511 | frameshift variant | TAAA/- | delins | 36 | |||
rs1801155 | 0.649 | 0.440 | 5 | 112839514 | missense variant | T/A | snv | 8.0E-06; 2.0E-03 | 1.2E-03 | 42 | |
rs459552 | 0.752 | 0.320 | 5 | 112841059 | missense variant | T/A;G | snv | 0.79 | 14 | ||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 93 | |||
rs16892766 | 0.716 | 0.240 | 8 | 116618444 | intergenic variant | A/C | snv | 9.3E-02 | 18 | ||
rs2770150 | 0.925 | 0.080 | 9 | 117700861 | upstream gene variant | A/G | snv | 0.22 | 4 | ||
rs10759932 | 0.732 | 0.560 | 9 | 117702866 | upstream gene variant | T/C | snv | 0.18 | 15 | ||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs11536898 | 0.882 | 0.080 | 9 | 117717932 | 3 prime UTR variant | C/A | snv | 0.14 | 3 |