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
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs6917
PHB
0.790 0.200 17 49404181 3 prime UTR variant G/A snv 0.16 7
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2302254 0.752 0.240 17 51153539 5 prime UTR variant C/T snv 0.22 15
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs4143815 0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23 20
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs4648068 0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2424913 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36