Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs10833 0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs236918 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs4374383 0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs3480 0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs10433937 0.882 0.080 4 87308948 intron variant T/A;C;G snv 4