Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11167764 | 0.925 | 0.120 | 5 | 142099500 | regulatory region variant | A/C | snv | 0.80 | 2 | ||
rs199883290 | 0.925 | 0.120 | 16 | 50729867 | missense variant | G/A;C | snv | 4.0E-06; 1.5E-02 | 7.0E-06 | 2 | |
rs2066847 | 0.716 | 0.400 | 16 | 50729868 | frameshift variant | C/-;CC | delins | 1.5E-02 | 2 | ||
rs224136 | 0.925 | 0.120 | 10 | 62710915 | intron variant | C/A;T | snv | 0.34 | 2 | ||
rs540973741 | 0.925 | 0.120 | 16 | 50729868 | frameshift variant | C/-;CC | delins | 2 | |||
rs5743293 | 0.807 | 0.200 | 16 | 50729868 | frameshift variant | C/-;CC | delins | 2 | |||
rs10045431 | 0.851 | 0.240 | 5 | 159387525 | intron variant | A/C | snv | 0.78 | 3 | ||
rs10995271 | 0.776 | 0.280 | 10 | 62678726 | downstream gene variant | G/C | snv | 0.32 | 3 | ||
rs11175593 | 0.882 | 0.160 | 12 | 40208138 | non coding transcript exon variant | C/T | snv | 2.8E-02 | 3 | ||
rs11465804 | 0.752 | 0.320 | 1 | 67236843 | intron variant | T/G | snv | 4.4E-02 | 5.4E-02 | 3 | |
rs11747270 | 0.790 | 0.240 | 5 | 150879305 | intron variant | A/G | snv | 0.21 | 3 | ||
rs1456893 | 0.851 | 0.160 | 7 | 50230076 | intron variant | G/A | snv | 0.69 | 3 | ||
rs1551398 | 0.882 | 0.160 | 8 | 125527809 | intron variant | G/A | snv | 0.48 | 3 | ||
rs17582416 | 0.882 | 0.160 | 10 | 34998722 | regulatory region variant | T/G | snv | 0.31 | 3 | ||
rs1847472 | 0.807 | 0.200 | 6 | 90263440 | intron variant | C/A | snv | 0.25 | 3 | ||
rs2274910 | 0.827 | 0.200 | 1 | 160882256 | non coding transcript exon variant | T/C | snv | 0.65 | 0.58 | 3 | |
rs3828309 | 0.882 | 0.160 | 2 | 233271764 | intron variant | A/G | snv | 0.42 | 3 | ||
rs4263839 | 0.807 | 0.160 | 9 | 114804160 | intron variant | A/G | snv | 0.75 | 3 | ||
rs4613763 | 0.851 | 0.240 | 5 | 40392626 | regulatory region variant | T/C | snv | 0.14 | 3 | ||
rs6908425 | 0.752 | 0.320 | 6 | 20728500 | intron variant | T/C | snv | 0.78 | 3 | ||
rs744166 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 3 | ||
rs762421 | 0.851 | 0.360 | 21 | 44195678 | intron variant | G/A | snv | 3 | |||
rs7746082 | 0.851 | 0.160 | 6 | 105987394 | regulatory region variant | G/A;C | snv | 3 | |||
rs8005161 | 0.882 | 0.120 | 14 | 88006251 | intron variant | C/T | snv | 0.18 | 3 | ||
rs11190140 | 0.827 | 0.160 | 10 | 99531836 | upstream gene variant | T/C | snv | 0.55 | 4 |