Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2071203 | 0.827 | 0.120 | 3 | 50274469 | missense variant | C/T | snv | 0.12 | 9.9E-02 | 6 | |
rs680055 | 0.851 | 0.120 | 7 | 99859982 | missense variant | C/A;G | snv | 6.5E-02 | 0.13 | 5 | |
rs7463708 | 0.807 | 0.120 | 8 | 127091810 | non coding transcript exon variant | G/T | snv | 0.27 | 7 | ||
rs7837328 | 0.882 | 0.120 | 8 | 127410882 | intron variant | A/G | snv | 0.52 | 8 | ||
rs7965399 | 0.851 | 0.120 | 12 | 102497908 | regulatory region variant | T/A;C | snv | 5 | |||
rs10090154 | 0.807 | 0.160 | 8 | 127519892 | intergenic variant | T/A;C | snv | 7 | |||
rs1012477 | 0.827 | 0.160 | 1 | 7798075 | intron variant | G/C | snv | 0.16 | 8 | ||
rs1042489 | 0.851 | 0.160 | 17 | 78224125 | 3 prime UTR variant | T/C | snv | 0.40 | 5 | ||
rs1290923018 | 0.851 | 0.160 | 11 | 65570699 | missense variant | G/A | snv | 4.0E-06 | 5 | ||
rs1512268 | 0.851 | 0.160 | 8 | 23668950 | intergenic variant | T/C | snv | 0.50 | 6 | ||
rs16901946 | 0.827 | 0.160 | 8 | 127088680 | non coding transcript exon variant | A/G | snv | 1.7E-02 | 8 | ||
rs1801320 | 0.742 | 0.160 | 15 | 40695330 | 5 prime UTR variant | G/C | snv | 0.12 | 15 | ||
rs1801321 | 0.790 | 0.160 | 15 | 40695367 | 5 prime UTR variant | G/C;T | snv | 0.35 | 8 | ||
rs1859962 | 0.882 | 0.160 | 17 | 71112612 | intron variant | G/T | snv | 0.56 | 4 | ||
rs2735839 | 0.827 | 0.160 | 19 | 50861367 | upstream gene variant | A/C;G | snv | 7 | |||
rs4792311 | 0.776 | 0.160 | 17 | 13011692 | missense variant | G/A;C | snv | 0.27 | 9 | ||
rs565453 | 0.882 | 0.160 | 5 | 112849696 | intron variant | A/C;G | snv | 4 | |||
rs605059 | 0.763 | 0.160 | 17 | 42554888 | missense variant | G/A;C;T | snv | 0.56; 9.0E-05; 1.4E-05 | 15 | ||
rs12338 | 0.807 | 0.200 | 8 | 11853379 | missense variant | G/A;C;T | snv | 8.0E-06; 0.38; 2.4E-05 | 10 | ||
rs3774262 | 0.851 | 0.200 | 3 | 186854025 | intron variant | G/A | snv | 0.10 | 5 | ||
rs864622007 | 0.882 | 0.200 | X | 67711621 | missense variant | T/A | snv | 5 | |||
rs138213197 | 0.701 | 0.240 | 17 | 48728343 | missense variant | C/T | snv | 1.8E-03 | 1.6E-03 | 24 | |
rs28366003 | 0.763 | 0.240 | 16 | 56608579 | upstream gene variant | A/C;G | snv | 4.6E-02 | 10 | ||
rs3822214 | 0.732 | 0.240 | 4 | 54727298 | missense variant | A/C;G;T | snv | 7.7E-02; 8.0E-06 | 13 | ||
rs4988483 | 0.752 | 0.240 | 16 | 1079010 | missense variant | C/A | snv | 3.7E-02 | 3.7E-02 | 11 |