Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2066845 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs2076530 0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 17
rs35947132 0.776 0.280 10 70600631 missense variant G/A snv 2.9E-02 2.9E-02 10
rs3811047 0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs3731865 0.882 0.160 2 218385280 non coding transcript exon variant G/A;C;T snv 0.23; 1.4E-04 5