Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111033563 0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 8
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1239681664 0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs11978267 0.763 0.240 7 50398606 intron variant A/G snv 0.25 9
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
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
rs387906659 0.742 0.280 19 40257052 stop gained C/A;T snv 14
rs35201683
HFE
0.732 0.360 6 26094205 stop gained C/A;T snv 1.4E-03 12
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs780246573 0.732 0.360 6 26092860 stop gained C/G;T snv 4.0E-06; 8.0E-06 12
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
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs397514606 0.763 0.320 1 243695714 missense variant C/T snv 14
rs1532268 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 12
rs1799929 0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36 11