Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3129871 0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs8878 0.827 0.280 4 76021147 3 prime UTR variant A/C;G snv 5
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs3134603 0.851 0.360 6 32158225 non coding transcript exon variant A/C;G;T snv 4
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1077393 0.882 0.200 6 31642752 non coding transcript exon variant A/G snv 0.44 3
rs10795791 0.925 0.200 10 6066377 upstream gene variant A/G snv 0.40 2
rs11229 0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs1214611 0.925 0.200 1 167479867 intron variant A/G snv 0.54 2
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12708716 0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs1270942 0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2239800 0.882 0.280 6 32745490 intron variant A/G snv 0.11 3
rs2260000 0.851 0.200 6 31625699 intron variant A/G snv 0.29 7
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2395157 0.827 0.240 6 32380368 intron variant A/G snv 0.24 5
rs2395173 0.882 0.240 6 32437082 upstream gene variant A/G snv 0.62 3
rs241409 0.925 0.200 6 32894143 upstream gene variant A/G snv 9.8E-02 2
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2844484 0.807 0.320 6 31568447 upstream gene variant A/G snv 0.64 6