Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
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
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
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
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs3742330 0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs3748067 0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02 21