Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1076064 0.851 0.160 5 149732603 intron variant A/G snv 0.47 4
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 47
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs864745 0.763 0.320 7 28140937 intron variant T/C snv 0.41 8
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs10012 0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42