Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs1553403917 0.807 0.320 2 73451171 frameshift variant -/A delins 7
rs2645424 0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs2294918 0.925 0.040 22 43946236 missense variant A/G snv 0.68 0.70 3
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs1057972 0.790 0.200 4 141733279 3 prime UTR variant A/T snv 0.54 7
rs1251713297 0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 15
rs12743824 0.925 0.040 1 99317401 intergenic variant C/A snv 0.48 2
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs2228603 0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs12784396 0.925 0.040 10 100267650 5 prime UTR variant C/A;T snv 4
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs626283 0.827 0.160 19 54173307 upstream gene variant C/G snv 0.61 7
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs779021719 0.827 0.120 19 35284962 stop gained C/G;T snv 9.1E-05 5
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42