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
rs11935941 1.000 0.040 4 148731326 intron variant A/C snv 0.31 2
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs4149570 0.752 0.360 12 6342424 upstream gene variant A/C;G;T snv 11
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs3850641 0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs10774625 0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs179247 0.882 0.160 14 80966202 intron variant A/G snv 0.40 5
rs30461 0.827 0.120 19 39298475 missense variant A/G snv 0.13 0.25 5
rs17759659 0.851 0.120 18 63291411 intron variant A/G snv 0.31 4
rs6543116 0.882 0.120 2 102311266 upstream gene variant A/G snv 0.76 3
rs7171171 0.925 0.120 15 38614840 intergenic variant A/G snv 0.24 3
rs7629750 0.882 0.040 3 119455829 intron variant A/G snv 0.45 3
rs853326
TG
0.882 0.120 8 132897729 missense variant A/G snv 0.58 0.60 3
rs1269486 0.925 0.120 10 8054236 intron variant A/G snv 0.77 2
rs2227478 0.925 0.040 12 68254842 upstream gene variant A/G snv 0.37 2
rs4411444 0.925 0.120 14 80978764 intron variant A/G snv 0.43 2
rs756763 1.000 0.040 17 51671952 intron variant A/G snv 0.48 2
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115