Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10885122 | 1.000 | 0.080 | 10 | 111282335 | intergenic variant | T/G | snv | 0.71 | 4 | ||
rs4458523 | 1.000 | 0.080 | 4 | 6288259 | intron variant | T/G | snv | 0.61 | 3 | ||
rs16913693 | 9 | 108918079 | intron variant | T/G | snv | 8.4E-02 | 2 | ||||
rs2300615 | 6 | 39071727 | intron variant | T/G | snv | 0.17 | 2 | ||||
rs3138708 | 3 | 171009914 | intron variant | T/G | snv | 3.1E-02 | 2 | ||||
rs983309 | 8 | 9320222 | intron variant | T/G | snv | 0.82 | 2 | ||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs3816725 | 11 | 47284118 | intron variant | T/C;G | snv | 2 | |||||
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 62 | ||
rs10811661 | 0.724 | 0.400 | 9 | 22134095 | intergenic variant | T/C | snv | 0.14 | 22 | ||
rs560887 | 0.827 | 0.120 | 2 | 168906638 | intron variant | T/C | snv | 0.79 | 0.80 | 18 | |
rs174550 | 0.925 | 0.160 | 11 | 61804006 | 5 prime UTR variant | T/C | snv | 0.28 | 13 | ||
rs2068834 | 0.925 | 0.120 | 2 | 27616672 | intron variant | T/C | snv | 0.28 | 10 | ||
rs2126259 | 1.000 | 8 | 9327636 | intron variant | T/C | snv | 0.87 | 9 | |||
rs340874 | 0.882 | 0.080 | 1 | 213985913 | non coding transcript exon variant | T/C | snv | 0.40 | 7 | ||
rs17265513 | 0.925 | 0.160 | 20 | 41203988 | missense variant | T/C | snv | 0.14 | 0.14 | 6 | |
rs2877716 | 3 | 123375604 | intron variant | T/C | snv | 0.76 | 4 | ||||
rs4502156 | 1.000 | 0.080 | 15 | 62090956 | intergenic variant | T/C | snv | 0.55 | 4 | ||
rs6975024 | 7 | 44192287 | intron variant | T/C | snv | 0.14 | 4 | ||||
rs11717195 | 1.000 | 0.080 | 3 | 123363551 | intron variant | T/C | snv | 0.19 | 3 | ||
rs12440695 | 15 | 62142957 | regulatory region variant | T/C | snv | 0.32 | 3 | ||||
rs1401419 | 1.000 | 0.040 | 11 | 45858188 | intron variant | T/C | snv | 0.39 | 3 | ||
rs4245555 | 1.000 | 0.120 | 7 | 50593712 | intron variant | T/C | snv | 0.32 | 3 | ||
rs11039182 | 11 | 47325172 | intron variant | T/C | snv | 0.19 | 2 | ||||
rs1280 | 3 | 170995501 | intron variant | T/C | snv | 0.20 | 2 |