Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs12952581 0.925 0.080 17 49370984 intron variant G/A snv 0.42 0.28 3
rs3785356 0.925 0.080 16 27337847 intron variant C/T snv 0.25 5
rs11071559 0.925 0.080 15 60777789 intron variant C/T snv 0.23 4
rs17293632 0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs2033784 1.000 0.080 15 67157322 intron variant A/G snv 0.35 4
rs8005161 0.882 0.120 14 88006251 intron variant C/T snv 0.18 5
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
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
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
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