Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5906435 1.000 0.040 X 47589011 intron variant C/G;T snv 1
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs12976445 0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs1800472 0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 11
rs3826782 0.882 0.040 19 6887725 intron variant G/A snv 8.6E-02 3
rs10404453 1.000 0.040 19 51693235 non coding transcript exon variant G/A;C snv 2.6E-03; 5.5E-06 1
rs6354 0.732 0.280 17 30222880 5 prime UTR variant G/C;T snv 16
rs2779249 0.851 0.200 17 27801555 intron variant C/A snv 0.33 7
rs12449783 1.000 0.040 17 30200635 intron variant A/C;T snv 1
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs224222 0.724 0.440 16 3254463 missense variant C/T snv 0.24 0.21 15
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs9533156 0.807 0.280 13 42573535 intron variant T/C snv 0.47 8
rs2277438 0.827 0.160 13 42581032 intron variant G/A;C snv 5
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81