Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
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
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs3734254 0.752 0.240 6 35427233 3 prime UTR variant C/T snv 0.69 14
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64