Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs515135 | 0.807 | 0.160 | 2 | 21063185 | intergenic variant | T/C | snv | 0.73 | 6 | ||
rs562338 | 0.807 | 0.160 | 2 | 21065449 | intergenic variant | A/G | snv | 0.69 | 6 | ||
rs12654264 | 0.925 | 0.120 | 5 | 75352778 | intron variant | A/T | snv | 0.38 | 5 | ||
rs16996148 | 0.882 | 0.120 | 19 | 19547663 | downstream gene variant | G/T | snv | 0.10 | 5 | ||
rs3846662 | 0.763 | 0.280 | 5 | 75355259 | non coding transcript exon variant | A/G | snv | 0.50 | 0.58 | 5 | |
rs6544713 | 0.925 | 0.040 | 2 | 43846742 | non coding transcript exon variant | T/C | snv | 0.75 | 5 | ||
rs11591147 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 4 | ||
rs12670798 | 1.000 | 0.040 | 7 | 21567734 | intron variant | T/C | snv | 0.26 | 4 | ||
rs3798220 | 0.732 | 0.160 | 6 | 160540105 | missense variant | T/C | snv | 5.6E-02 | 3.1E-02 | 4 | |
rs3846663 | 0.882 | 0.120 | 5 | 75359901 | intron variant | C/T | snv | 0.35 | 4 | ||
rs6756629 | 0.925 | 0.080 | 2 | 43837951 | missense variant | G/A;T | snv | 6.7E-02 | 4 | ||
rs1501908 | 1.000 | 0.040 | 5 | 156971158 | intergenic variant | G/A;C;T | snv | 3 | |||
rs2254287 | 1.000 | 0.040 | 6 | 33176171 | intron variant | C/A;G;T | snv | 3 | |||
rs4844614 | 1.000 | 0.040 | 1 | 207701830 | intron variant | G/C;T | snv | 3 | |||
rs5031002 | 1.000 | 0.040 | X | 67722783 | intron variant | G/A | snv | 1.5E-02 | 1.5E-02 | 3 | |
rs6102059 | 1.000 | 0.040 | 20 | 40600144 | intergenic variant | C/T | snv | 0.33 | 3 | ||
rs7703051 | 0.851 | 0.120 | 5 | 75329662 | intron variant | C/A | snv | 0.38 | 3 |