Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10866713 | 1.000 | 0.080 | 5 | 159491886 | intron variant | G/A | snv | 0.16 | 1 | ||
rs10876994 | 0.925 | 0.120 | 12 | 57670954 | upstream gene variant | A/C;T | snv | 1 | |||
rs11129295 | 1.000 | 0.080 | 3 | 27747289 | intergenic variant | C/T | snv | 0.39 | 1 | ||
rs11594656 | 0.776 | 0.240 | 10 | 6080046 | intergenic variant | T/A | snv | 0.18 | 1 | ||
rs12048904 | 1.000 | 0.080 | 1 | 100865980 | intergenic variant | T/C | snv | 0.48 | 1 | ||
rs12087340 | 1.000 | 0.080 | 1 | 85281310 | intron variant | C/T | snv | 8.4E-02 | 1 | ||
rs12296430 | 1.000 | 0.080 | 12 | 6394334 | splice region variant | G/C | snv | 0.16 | 1 | ||
rs13192841 | 0.925 | 0.120 | 6 | 137646077 | intergenic variant | G/A | snv | 0.24 | 1 | ||
rs13333054 | 1.000 | 0.080 | 16 | 85977427 | intron variant | C/A;T | snv | 1 | |||
rs1356122 | 1.000 | 0.080 | 3 | 154465773 | intergenic variant | G/A;C | snv | 1 | |||
rs1401884 | 1.000 | 0.080 | 16 | 85979945 | intron variant | G/C | snv | 0.18 | 1 | ||
rs1438131 | 1.000 | 0.080 | 2 | 23283911 | regulatory region variant | G/A | snv | 0.34 | 1 | ||
rs1610630 | 1.000 | 0.080 | 6 | 29761509 | intron variant | C/T | snv | 0.81 | 1 | ||
rs1633069 | 1.000 | 0.080 | 6 | 29756424 | intron variant | C/G | snv | 0.81 | 1 | ||
rs1633070 | 1.000 | 0.080 | 6 | 29756370 | intron variant | T/A;C | snv | 1 | |||
rs17066096 | 1.000 | 0.080 | 6 | 137131771 | intergenic variant | A/G | snv | 0.20 | 1 | ||
rs1737060 | 1.000 | 0.080 | 6 | 29765192 | upstream gene variant | G/C | snv | 0.79 | 1 | ||
rs1737068 | 1.000 | 0.080 | 6 | 29763146 | non coding transcript exon variant | C/A | snv | 0.81 | 1 | ||
rs1843938 | 1.000 | 0.080 | 7 | 3073400 | intergenic variant | G/A | snv | 0.42 | 1 | ||
rs201847125 | 1.000 | 0.080 | 7 | 50285971 | intergenic variant | C/T | snv | 1 | |||
rs2157082 | 1.000 | 0.080 | 6 | 32792937 | intergenic variant | G/A;C;T | snv | 1 | |||
rs2163226 | 1.000 | 0.080 | 2 | 43134117 | upstream gene variant | T/C | snv | 0.33 | 1 | ||
rs2182410 | 1.000 | 0.080 | 10 | 6080706 | intergenic variant | T/A;C | snv | 1 | |||
rs233100 | 1.000 | 0.080 | 1 | 85306326 | intron variant | G/A | snv | 0.40 | 1 | ||
rs2516460 | 1.000 | 0.080 | 6 | 31450923 | intron variant | T/A;C;G | snv | 0.54 | 1 |