Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs744373 | 0.851 | 0.160 | 2 | 127137039 | downstream gene variant | A/G | snv | 0.35 | 8 | ||
rs2949506 | 0.851 | 0.160 | 18 | 30217168 | intergenic variant | C/T | snv | 0.14 | 5 | ||
rs200538373 | 0.925 | 0.120 | 19 | 1061893 | splice region variant | G/A;C | snv | 2.5E-03 | 2 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs201564694 | 0.882 | 0.120 | 1 | 159588626 | missense variant | T/C | snv | 3 | |||
rs1217777010 | 1.000 | 0.040 | 11 | 116836182 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs781049584 | 0.724 | 0.280 | 21 | 26021917 | missense variant | T/G | snv | 8.2E-06 | 7.0E-06 | 18 | |
rs572842823 | 0.763 | 0.160 | 21 | 25897626 | missense variant | T/A;G | snv | 11 | |||
rs371425292 | 0.763 | 0.160 | 21 | 25897627 | missense variant | C/A;T | snv | 8.0E-06 | 10 | ||
rs63750847 | 0.790 | 0.120 | 21 | 25897620 | missense variant | C/T | snv | 4.5E-04 | 3.0E-04 | 8 | |
rs63751039 | 0.776 | 0.200 | 21 | 25891855 | missense variant | T/C | snv | 8 | |||
rs950592627 | 0.827 | 0.200 | 21 | 26090015 | missense variant | G/C | snv | 7.0E-06 | 5 | ||
rs529782627 | 0.882 | 0.120 | 21 | 26112051 | missense variant | C/A | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs763852444 | 0.882 | 0.120 | 21 | 26112127 | missense variant | G/C | snv | 4.0E-06 | 3 | ||
rs10097505 | 0.925 | 0.120 | 8 | 142612823 | 3 prime UTR variant | G/A | snv | 0.47 | 2 | ||
rs73956431 | 0.827 | 0.120 | 18 | 31699870 | regulatory region variant | C/T | snv | 8.4E-02 | 6 | ||
rs970866 | 0.851 | 0.160 | 18 | 31681955 | intron variant | C/T | snv | 0.89 | 4 | ||
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs140226130 | 0.790 | 0.200 | 18 | 33336845 | intron variant | -/CTTTTTGCT | delins | 7.8E-02 | 8 | ||
rs2279590 | 0.851 | 0.200 | 8 | 27598736 | non coding transcript exon variant | T/C | snv | 0.69 | 5 | ||
rs7982 | 1.000 | 0.040 | 8 | 27604964 | missense variant | A/C;G | snv | 0.64 | 0.60 | 1 | |
rs9331888 | 0.827 | 0.200 | 8 | 27611345 | 5 prime UTR variant | C/G | snv | 0.35 | 0.28 | 5 | |
rs6656401 | 0.776 | 0.200 | 1 | 207518704 | intron variant | A/G;T | snv | 8 | |||
rs28939068 | 0.790 | 0.200 | 20 | 23635330 | missense variant | A/T | snv | 9 |