Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs3745274 0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs387906659 0.742 0.280 19 40257052 stop gained C/A;T snv 14
rs9904341 0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs8073069 0.807 0.200 17 78213692 upstream gene variant G/C snv 0.33 7
rs1325757098 0.827 0.160 16 71576223 missense variant C/T snv 8.0E-06 7.0E-06 6
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs2239633 0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 12
rs1057519766 0.851 0.080 13 28028203 missense variant G/C;T snv 5
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1239681664 0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs2230724 0.851 0.120 9 5081780 synonymous variant G/A snv 0.53 0.62 4
rs1801280 0.716 0.440 8 18400344 missense variant T/C snv 0.38 0.39 14
rs1799929 0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36 11
rs1470755915 0.776 0.240 8 92005229 missense variant C/A snv 7.0E-06 10
rs927698341 0.776 0.240 8 92005280 synonymous variant C/A snv 4.0E-06 2.8E-05 10
rs62527607 0.827 0.160 8 103141321 non coding transcript exon variant G/T snv 0.14 5