Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12144049 | 1.000 | 0.120 | 1 | 152468434 | intergenic variant | C/G;T | snv | 1 | |||
rs12153855 | 0.776 | 0.320 | 6 | 32107027 | intron variant | T/C | snv | 0.11 | 11 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs12188917 | 1.000 | 0.120 | 5 | 132655393 | intron variant | T/C;G | snv | 1 | |||
rs121909626 | 0.882 | 0.120 | 1 | 152307225 | stop gained | G/C;T | snv | 2.0E-05 | 4 | ||
rs12198173 | 0.827 | 0.240 | 6 | 32059031 | intron variant | G/A | snv | 0.10 | 9 | ||
rs12211410 | 0.925 | 0.120 | 6 | 32081646 | missense variant | C/G;T | snv | 5.6E-05; 7.7E-02; 3.7E-05 | 5 | ||
rs1221479287 | 0.925 | 0.120 | 19 | 54783499 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
rs1239828657 | 0.925 | 0.120 | 9 | 6256028 | missense variant | T/G | snv | 4.0E-06 | 2 | ||
rs12568784 | 0.925 | 0.120 | 1 | 152350656 | stop gained | G/A;T | snv | 0.24 | 0.21 | 2 | |
rs12634229 | 0.882 | 0.120 | 3 | 112657461 | intergenic variant | T/C | snv | 0.15 | 3 | ||
rs1295685 | 0.790 | 0.160 | 5 | 132660753 | 3 prime UTR variant | A/G | snv | 0.81 | 7 | ||
rs1295686 | 0.882 | 0.160 | 5 | 132660151 | intron variant | T/A;C | snv | 0.68 | 7 | ||
rs13015714 | 0.882 | 0.200 | 2 | 102355405 | intron variant | G/T | snv | 0.77 | 3 | ||
rs13132933 | 0.925 | 0.200 | 4 | 122089432 | upstream gene variant | T/C | snv | 0.22 | 2 | ||
rs13139310 | 0.925 | 0.120 | 4 | 184435757 | intron variant | G/A;C | snv | 3 | |||
rs13199524 | 0.807 | 0.240 | 6 | 32098988 | intron variant | C/T | snv | 8.4E-02 | 9 | ||
rs1335908042 | 0.925 | 0.120 | 2 | 112918756 | missense variant | T/G | snv | 4.0E-06 | 2 | ||
rs13360927 | 0.882 | 0.160 | 5 | 110700055 | intron variant | A/G | snv | 9.3E-02 | 3 | ||
rs13361382 | 0.882 | 0.160 | 5 | 110713253 | intron variant | G/A | snv | 9.3E-02 | 3 | ||
rs1343795 | 0.882 | 0.120 | 17 | 49334880 | intron variant | C/A | snv | 0.78 | 5 | ||
rs1384974 | 0.925 | 0.120 | 3 | 177009491 | downstream gene variant | T/C | snv | 9.6E-02 | 2 | ||
rs138726443 | 0.790 | 0.200 | 1 | 152307547 | stop gained | G/A;C;T | snv | 2.8E-03; 4.0E-06; 1.6E-05 | 7 | ||
rs1422985 | 0.925 | 0.120 | 5 | 148114596 | intron variant | A/C | snv | 3.2E-02 | 2 | ||
rs1443712053 | 0.925 | 0.120 | 1 | 152310672 | stop gained | G/C | snv | 4.0E-06 | 2 |