Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2814778 0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 24
rs1420101 0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 8
rs34290285 0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs9807989 1.000 0.080 2 102354740 intron variant T/C;G snv 0.46 2
rs10455025 1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 3
rs16903574 0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs2416257 0.882 0.160 5 111099792 intron variant C/G;T snv 5
rs4594881 1.000 0.080 5 35846713 intergenic variant G/T snv 0.28 2
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 4
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs10905284 0.882 0.200 10 8073399 intron variant C/A;T snv 4
rs12722502 0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs1444782 0.851 0.240 10 9016708 intergenic variant G/A snv 0.35 5
rs61840192 1.000 0.080 10 9001441 intergenic variant G/A;C;T snv 3
rs7918084 1.000 0.080 10 92669710 non coding transcript exon variant C/T snv 0.60 3
rs11603634 1.000 0.080 11 1142570 intergenic variant A/G snv 0.38 2
rs55646091 0.925 0.080 11 76588387 upstream gene variant G/A snv 3.0E-02 5
rs61894547 0.882 0.160 11 76537586 intron variant C/T snv 3.1E-02 4
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs1059513 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs3024971 0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 7