Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737 0.679 0.107 12 2236129 intron variant G/A snp 0.37 13
rs6265 0.463 0.679 11 27658369 missense variant C/T snp 0.19 0.15 5
rs113378111 1.000 0.036 2 9788024 regulatory region variant G/A snp 3.3E-02 3
rs114465512 1.000 0.036 22 22047895 C/T snp 3.8E-03 3
rs1994321 1.000 0.036 11 12065766 intergenic variant G/T snp 0.32 3
rs150175932 1.000 0.036 4 150101495 intron variant T/C snp 2.1E-02 3
rs80164876 1.000 0.036 5 38464142 3 prime UTR variant A/G snp 2.0E-02 3
rs117198528 1.000 0.036 18 49694188 intergenic variant T/G snp 1.1E-02 3
rs2251219 0.734 0.071 3 52550771 synonymous variant T/C snp 0.39; 4.0E-06 0.34 3
rs662 0.561 0.607 7 95308134 missense variant T/C snp 0.38 0.41 3
rs35863382 1.000 0.036 14 91472532 intron variant C/T snp 5.9E-02 3
rs111365677 1.000 0.036 1 99463578 intergenic variant T/C snp 2.2E-03 2
rs112538845 1.000 0.036 4 184084475 intergenic variant C/T snp 1.8E-02 2
rs143934587 1.000 0.036 20 19165806 G/A snp 9.0E-03 2
rs189864513 1.000 0.036 4 52767390 T/C snp 1.4E-03 2
rs190544851 1.000 0.036 21 38360474 intergenic variant T/G snp 5.5E-03 2
rs190783615 1.000 0.036 X 142772620 T/C snp 1.0E-02 2
rs1908557 1.000 0.036 4 89500202 intergenic variant T/C snp 0.31; 3.2E-05 2
rs201569130 1.000 0.036 6 1402916 intergenic variant CACAG/C in-del 2
rs201921722 1.000 0.036 11 123679999 T/TA in-del 2
rs34807503 1.000 0.036 12 51525350 intergenic variant CATTT/C in-del 2
rs56388524 1.000 0.036 5 45757459 intergenic variant C/T snp 2.9E-02 2
rs74860738 1.000 0.036 11 80671683 intergenic variant G/A snp 7.6E-02 2
rs75995702 1.000 0.036 11 42785177 intergenic variant C/G,T snp 4.5E-03; 3.2E-05 2
rs78087832 1.000 0.036 2 224600060 intergenic variant C/T snp 2.9E-03 2