Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs629849 0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 9
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs2287622 0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2298839
AFP
0.925 0.080 4 73445127 splice region variant A/G;T snv 0.54 2
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs6591182 0.925 0.080 11 65582285 missense variant T/G snv 0.47 0.45 2
rs4898 0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs886277 1.000 0.080 11 2418537 missense variant T/C snv 0.44 0.47 1
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs5744174 0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs2241883 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs3775290 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 15