Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs3745274 0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 19
rs1801280 0.716 0.440 8 18400344 missense variant T/C snv 0.38 0.39 14
rs397514606 0.763 0.320 1 243695714 missense variant C/T snv 13
rs1532268 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 12
rs1470755915 0.776 0.240 8 92005229 missense variant C/A snv 7.0E-06 10
rs111033563 0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 8
rs1325757098 0.827 0.160 16 71576223 missense variant C/T snv 8.0E-06 7.0E-06 6
rs1057519766 0.851 0.080 13 28028203 missense variant G/C;T snv 5
rs751689316 0.925 0.080 3 169131510 missense variant C/T snv 1.2E-05 4
rs777017502 0.925 0.080 2 37222420 missense variant T/C;G snv 4.2E-06; 4.2E-06 3
rs62527607 0.827 0.160 8 103141321 non coding transcript exon variant G/T snv 0.14 5
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1239681664 0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs1799929 0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36 11
rs927698341 0.776 0.240 8 92005280 synonymous variant C/A snv 4.0E-06 2.8E-05 10
rs2230724 0.851 0.120 9 5081780 synonymous variant G/A snv 0.53 0.62 4
rs9904341 0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs4132601 0.763 0.240 7 50402906 3 prime UTR variant T/G snv 0.25 6
rs767464424 0.925 0.080 2 37222420 frameshift variant T/- delins 4.2E-06 3
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 98
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs2239633 0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 8
rs8073069 0.807 0.200 17 78213692 upstream gene variant G/C snv 0.33 7