Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs53576 | 0.641 | 0.320 | 3 | 8762685 | intron variant | A/G;T | snv | 42 | |||
rs6318 | 0.623 | 0.520 | X | 114731326 | missense variant | C/G;T | snv | 42 | |||
rs110402 | 0.790 | 0.120 | 17 | 45802681 | intron variant | G/A;C | snv | 12 | |||
rs356219 | 0.776 | 0.240 | 4 | 89716450 | intron variant | G/A | snv | 0.54 | 9 | ||
rs7958822 | 0.807 | 0.200 | 12 | 27348173 | intron variant | G/A | snv | 0.43 | 6 | ||
rs279871 | 0.882 | 0.080 | 4 | 46303716 | intron variant | T/C | snv | 0.38 | 5 | ||
rs17153694 | 0.851 | 0.160 | 8 | 11730972 | intron variant | C/T | snv | 0.12 | 4 | ||
rs2306073 | 0.882 | 0.080 | 12 | 27402904 | intron variant | C/T | snv | 0.37 | 4 | ||
rs356200 | 0.882 | 0.160 | 4 | 89747463 | intron variant | T/C | snv | 0.44 | 4 | ||
rs3782025 | 0.882 | 0.080 | 11 | 113936885 | intron variant | G/A | snv | 0.55 | 4 | ||
rs10112596 | 0.925 | 0.120 | 8 | 11722293 | intron variant | A/G | snv | 0.83 | 3 | ||
rs2412646 | 0.882 | 0.120 | 4 | 55452605 | 3 prime UTR variant | T/C | snv | 0.58 | 3 | ||
rs463379 | 0.882 | 0.080 | 5 | 1431049 | intron variant | G/C | snv | 0.31 | 3 | ||
rs4964057 | 0.882 | 0.080 | 12 | 27363909 | intron variant | T/G | snv | 0.29 | 3 | ||
rs11240 | 0.925 | 0.080 | 4 | 55453183 | 3 prime UTR variant | C/A;G | snv | 2 | |||
rs11941860 | 1.000 | 0.080 | 4 | 46080161 | intron variant | C/T | snv | 0.12 | 2 | ||
rs2119183 | 1.000 | 0.080 | 4 | 46270789 | intron variant | G/A | snv | 7.6E-02 | 2 | ||
rs3756007 | 1.000 | 0.080 | 4 | 46389047 | 5 prime UTR variant | T/C | snv | 5.4E-02 | 2 | ||
rs3811939 | 1.000 | 0.080 | 5 | 76954762 | intron variant | G/A | snv | 0.27 | 2 | ||
rs536599 | 1.000 | 0.080 | 4 | 46196917 | intergenic variant | G/T | snv | 0.47 | 2 | ||
rs56013859 | 0.925 | 0.080 | 2 | 238276865 | intron variant | T/C | snv | 0.11 | 2 | ||
rs6473797 | 0.925 | 0.080 | 8 | 53240422 | intron variant | T/C | snv | 0.39 | 2 | ||
rs10044881 | 1.000 | 0.080 | 5 | 148645656 | non coding transcript exon variant | T/C | snv | 0.17 | 1 | ||
rs10405681 | 1.000 | 0.080 | 19 | 3634021 | intron variant | C/A;T | snv | 1 | |||
rs10419980 | 1.000 | 0.080 | 19 | 3685118 | intron variant | C/T | snv | 0.29 | 1 |