Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4845618 | 0.851 | 0.160 | 1 | 154427539 | intron variant | G/T | snv | 0.53 | 5 | ||
rs12083537 | 0.882 | 0.200 | 1 | 154408627 | intron variant | A/G | snv | 0.22 | 4 | ||
rs4845623 | 0.925 | 0.040 | 1 | 154443301 | intron variant | A/G | snv | 0.47 | 4 | ||
rs61812598 | 1.000 | 0.080 | 1 | 154447611 | intron variant | G/A | snv | 0.31 | 4 | ||
rs7518199 | 1 | 154434943 | intron variant | A/C;T | snv | 0.39; 4.2E-06 | 4 | ||||
rs12034383 | 1 | 207630250 | intron variant | G/A | snv | 0.47 | 3 | ||||
rs12133641 | 0.925 | 0.040 | 1 | 154455807 | intron variant | A/G | snv | 0.44 | 3 | ||
rs12741825 | 1 | 159700355 | downstream gene variant | C/T | snv | 0.24 | 3 | ||||
rs12753193 | 1 | 65703996 | non coding transcript exon variant | G/A | snv | 0.58 | 3 | ||||
rs2808629 | 0.925 | 0.160 | 1 | 159707006 | upstream gene variant | G/A | snv | 0.31 | 3 | ||
rs3027012 | 1 | 159204333 | 5 prime UTR variant | C/T | snv | 0.13 | 3 | ||||
rs3093068 | 1.000 | 0.040 | 1 | 159711574 | downstream gene variant | G/C | snv | 0.13 | 3 | ||
rs4660808 | 1 | 39552837 | intron variant | C/T | snv | 0.17 | 3 | ||||
rs661955 | 1 | 234707109 | upstream gene variant | G/C;T | snv | 3 | |||||
rs7549785 | 0.925 | 0.080 | 1 | 159308078 | 3 prime UTR variant | G/A | snv | 0.13 | 3 | ||
rs876537 | 1.000 | 0.080 | 1 | 159705143 | non coding transcript exon variant | C/T | snv | 0.34 | 3 | ||
rs10908713 | 1 | 159369769 | intron variant | T/C | snv | 0.47 | 2 | ||||
rs11208722 | 1 | 65705318 | intron variant | C/A | snv | 0.75 | 2 | ||||
rs11265174 | 1 | 159350569 | intron variant | T/A | snv | 0.35 | 2 | ||||
rs11265190 | 1 | 159421611 | intron variant | G/A | snv | 0.47 | 2 | ||||
rs11265191 | 1 | 159430569 | intron variant | C/G;T | snv | 2 | |||||
rs11265196 | 1 | 159448422 | intron variant | G/A | snv | 0.47 | 2 | ||||
rs11265260 | 1.000 | 0.080 | 1 | 159730249 | intergenic variant | A/G | snv | 6.8E-02 | 2 | ||
rs11265263 | 1 | 159740727 | intergenic variant | C/A;T | snv | 2 | |||||
rs1127311 | 1 | 154584187 | 3 prime UTR variant | G/A | snv | 0.42 | 2 |