Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs2855812 0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs3129878 0.807 0.360 6 32440958 intron variant A/C snv 0.30 6
rs3129943 0.851 0.240 6 32370918 intron variant A/G snv 0.26 4
rs4505848 0.776 0.400 4 122211337 intron variant A/G snv 0.29 8
rs6908425 0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs7044343 0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs740347 0.925 0.160 7 34772690 intron variant G/A;C;T snv 2
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs881375 0.925 0.160 9 120890620 intron variant T/C snv 0.68 2
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs9268644 0.827 0.360 6 32440267 intron variant A/C snv 0.68 5
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs9272346 0.790 0.320 6 32636595 intron variant G/A snv 0.54 8
rs9372120 0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs987870 0.851 0.160 6 33075103 intron variant A/G snv 0.19 4