Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
rs2066844 | 0.587 | 0.520 | 16 | 50712015 | missense variant | C/T | snv | 2.6E-02 | 2.9E-02 | 54 | |
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 46 | ||
rs2066845 | 0.611 | 0.600 | 16 | 50722629 | missense variant | G/C;T | snv | 1.1E-02; 2.2E-04 | 46 | ||
rs1799969 | 0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 | 38 | |
rs396991 | 0.742 | 0.480 | 1 | 161544752 | missense variant | A/C;G;T | snv | 0.33; 4.1E-06 | 14 | ||
rs2075820 | 0.790 | 0.200 | 7 | 30452621 | missense variant | C/T | snv | 0.27 | 0.28 | 10 | |
rs397514767 | 0.807 | 0.240 | 11 | 33710247 | missense variant | C/T | snv | 4.0E-06 | 7 | ||
rs1445335859 | 0.851 | 0.240 | X | 15331662 | missense variant | T/C | snv | 9.4E-06 | 5 | ||
rs1253159682 | 1.000 | 0.080 | 1 | 158255333 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
rs746073437 | 1.000 | 0.080 | 1 | 158356780 | missense variant | G/C | snv | 4.0E-06 | 1 | ||
rs762142186 | 1.000 | 0.080 | 1 | 161624600 | missense variant | C/G;T | snv | 4.0E-06 | 1 |