Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs148696809 0.851 0.160 6 28966575 downstream gene variant T/C snv 5.3E-02 4
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs2066847 0.716 0.400 16 50729868 frameshift variant C/-;CC delins 1.5E-02 18
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs3021097 0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs568404 0.851 0.120 10 129233875 regulatory region variant C/A;G;T snv 4
rs568408 0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49