Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10020288 | 1.000 | 0.040 | 4 | 28686220 | intergenic variant | G/A | snv | 0.38 | 2 | ||
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 7 | ||
rs10144845 | 1.000 | 0.040 | 14 | 74771067 | intron variant | C/T | snv | 0.62 | 2 | ||
rs10156548 | 1.000 | 0.040 | 9 | 23318435 | intron variant | G/C;T | snv | 2 | |||
rs10405382 | 1.000 | 0.040 | 19 | 32405810 | 5 prime UTR variant | C/G | snv | 0.18 | 2 | ||
rs10429537 | 1.000 | 0.040 | 9 | 23346844 | intron variant | C/G | snv | 0.33 | 2 | ||
rs1055447 | 1.000 | 0.040 | 11 | 47164873 | 3 prime UTR variant | C/A;T | snv | 2 | |||
rs10891564 | 1.000 | 0.040 | 11 | 113503291 | intergenic variant | G/A | snv | 0.34 | 2 | ||
rs10950393 | 1.000 | 0.040 | 7 | 12223920 | intron variant | T/C | snv | 0.50 | 2 | ||
rs10965780 | 1.000 | 0.040 | 9 | 23341717 | intron variant | C/G;T | snv | 3 | |||
rs10994336 | 0.776 | 0.160 | 10 | 60420054 | intron variant | C/T | snv | 7.5E-02 | 2 | ||
rs11039149 | 0.827 | 0.280 | 11 | 47255124 | intron variant | A/G | snv | 0.19 | 2 | ||
rs11039409 | 1.000 | 0.040 | 11 | 47814169 | intron variant | A/C | snv | 0.22 | 2 | ||
rs11123857 | 2 | 100987350 | non coding transcript exon variant | A/G | snv | 0.29 | 1 | ||||
rs111365677 | 0.925 | 0.040 | 1 | 99463578 | upstream gene variant | T/C | snv | 2.3E-03 | 3 | ||
rs11152363 | 1.000 | 0.040 | 18 | 55389957 | intron variant | G/A | snv | 0.16 | 2 | ||
rs11209175 | 1.000 | 0.040 | 1 | 67909145 | intron variant | C/T | snv | 0.54 | 2 | ||
rs112106319 | 0.925 | 0.040 | 9 | 115094539 | intron variant | A/T | snv | 2.8E-03 | 3 | ||
rs11214589 | 1.000 | 0.040 | 11 | 113374326 | intron variant | G/A | snv | 0.36 | 2 | ||
rs11214607 | 1.000 | 0.040 | 11 | 113441417 | intron variant | T/G | snv | 0.16 | 2 | ||
rs112538845 | 0.925 | 0.040 | 4 | 184084475 | downstream gene variant | C/T | snv | 1.7E-02 | 3 | ||
rs113378111 | 1.000 | 0.040 | 2 | 9788024 | intergenic variant | G/A | snv | 2.8E-02 | 3 | ||
rs114465512 | 1.000 | 0.040 | 22 | 22047895 | intron variant | C/T | snv | 4.7E-03 | 3 | ||
rs11514731 | 1.000 | 0.040 | 7 | 2011868 | intron variant | C/G | snv | 0.16 | 2 | ||
rs11599236 | 1.000 | 0.040 | 10 | 104694914 | intron variant | T/C;G | snv | 2 |