Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
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
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46