Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs139029625 | 0.827 | 0.120 | 19 | 41010006 | missense variant | G/A;C;T | snv | 2.8E-05; 4.5E-04; 8.0E-06 | 5 | ||
rs1408630981 | 0.827 | 0.120 | 7 | 55205492 | missense variant | C/G | snv | 4.0E-06 | 5 | ||
rs1800264 | 0.827 | 0.120 | X | 32699141 | missense variant | A/C;G | snv | 5.5E-06; 8.3E-03 | 5 | ||
rs3134615 | 0.827 | 0.120 | 1 | 39896394 | 3 prime UTR variant | C/A | snv | 0.17 | 5 | ||
rs375275361 | 0.827 | 0.120 | 17 | 7675054 | missense variant | A/G;T | snv | 1.2E-05; 4.0E-06 | 5 | ||
rs3816358 | 0.827 | 0.120 | 11 | 13369925 | intron variant | C/A;T | snv | 5 | |||
rs3842530 | 0.827 | 0.120 | 1 | 209432292 | non coding transcript exon variant | GCAGCAGCAGCAGCAGCAGCAGCAGCA/-;GCA;GCAGCA;GCAGCAGCA;GCAGCAGCAGCA;GCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA | delins | 5 | |||
rs4246742 | 0.827 | 0.120 | 5 | 1267241 | intron variant | T/A | snv | 0.23 | 5 | ||
rs6413432 | 0.827 | 0.120 | 10 | 133535040 | intron variant | T/A | snv | 9.9E-02 | 5 | ||
rs757163626 | 0.827 | 0.120 | 22 | 19962726 | missense variant | C/T | snv | 1.6E-05 | 7.0E-06 | 5 | |
rs10514231 | 0.807 | 0.160 | 5 | 82011593 | intron variant | C/T | snv | 0.56 | 6 | ||
rs12443621 | 0.807 | 0.120 | 16 | 52514125 | intron variant | A/G | snv | 0.48 | 6 | ||
rs1864182 | 0.827 | 0.120 | 5 | 82253421 | missense variant | C/A;G | snv | 0.59 | 0.47 | 6 | |
rs2736108 | 0.807 | 0.160 | 5 | 1297373 | upstream gene variant | C/T | snv | 0.24 | 6 | ||
rs3816360 | 0.807 | 0.120 | 11 | 13346203 | intron variant | T/C | snv | 0.58 | 6 | ||
rs5744533 | 0.807 | 0.120 | 5 | 75510279 | intron variant | C/A;T | snv | 6 | |||
rs624366 | 0.827 | 0.120 | 11 | 108283370 | intron variant | G/C | snv | 0.52 | 6 | ||
rs12203582 | 0.827 | 0.120 | 6 | 52240759 | intron variant | G/A;T | snv | 7 | |||
rs200847762 | 0.790 | 0.160 | 6 | 32129371 | missense variant | G/A | snv | 2.7E-04 | 1.4E-05 | 7 | |
rs2240688 | 0.790 | 0.160 | 4 | 15968726 | 3 prime UTR variant | T/G | snv | 0.22 | 7 | ||
rs3104746 | 0.790 | 0.120 | 16 | 52567188 | intron variant | T/A | snv | 8.6E-02 | 7 | ||
rs3219484 | 0.807 | 0.160 | 1 | 45334484 | missense variant | C/A;T | snv | 4.8E-02 | 4.8E-02 | 7 | |
rs587782596 | 0.807 | 0.200 | 17 | 7675071 | missense variant | G/A;T | snv | 7 | |||
rs1214285376 | 0.776 | 0.200 | 19 | 43543490 | missense variant | G/T | snv | 4.0E-06 | 8 | ||
rs17021918 | 0.776 | 0.240 | 4 | 94641726 | intron variant | C/T | snv | 0.30 | 8 |