Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs140504 0.882 0.040 22 23285182 missense variant A/G snv 0.81 0.86 3
rs12476147 0.851 0.040 2 184936178 missense variant A/T snv 0.66 0.59 4
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1137070 0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs4290270 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs7305115 0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs208294 0.790 0.320 12 121162450 missense variant T/A;C;G snv 0.51 9
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2522833 0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 7
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs6691840 0.827 0.120 1 36859876 missense variant A/C;G snv 0.27; 9.2E-05 5
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs6320 0.925 0.040 7 155070911 synonymous variant T/A;G snv 0.26; 1.2E-05 2
rs821616 0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs3810950 0.882 0.080 10 49616573 missense variant G/A snv 0.21 0.18 3