Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
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
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs10774671 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14