Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9976767 0.882 0.200 21 42416281 intron variant A/G snv 0.45 3
rs9275328 0.851 0.240 6 32699045 intergenic variant C/T snv 0.16 4
rs9262143 0.851 0.240 6 30685004 missense variant C/G;T snv 4.1E-06; 6.1E-02 4
rs9261290 0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs907715 0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs886424 0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 10
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs8192591 0.882 0.160 6 32218019 missense variant C/T snv 2.5E-02 2.2E-02 6
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs805294 0.882 0.240 6 31720440 intron variant A/G snv 0.48 3
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs7775397 0.790 0.400 6 32293475 missense variant T/G snv 6.0E-02 6.4E-02 7
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs7758736 0.882 0.200 6 32790617 intergenic variant G/A snv 0.14 3
rs7750641 0.807 0.360 6 31161533 missense variant C/T snv 7.0E-02 7.6E-02 6
rs7745656 0.882 0.200 6 32713193 upstream gene variant G/T snv 0.29 3
rs7731626 0.716 0.240 5 56148856 intron variant G/A snv 0.30 16
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 16
rs77150043 0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21