Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3129962 0.925 0.200 6 32411606 upstream gene variant G/A;C snv 2
rs3130618 0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 7
rs3134603 0.851 0.360 6 32158225 non coding transcript exon variant A/C;G;T snv 4
rs3134943 0.882 0.240 6 32179984 intron variant T/A;C snv 0.89 3
rs377763 0.925 0.200 6 32231367 intergenic variant C/A;T snv 2
rs3789604 0.776 0.360 1 113812320 synonymous variant T/A;C;G snv 8.5E-06; 1.3E-05; 0.17 9
rs3806156 0.827 0.280 6 32405921 intron variant G/A;T snv 5
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs412657 0.882 0.240 6 32243308 intergenic variant T/C;G snv 3
rs4760648
VDR
0.851 0.200 12 47886882 intron variant C/A;G;T snv 4
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs6903608 0.742 0.400 6 32460508 intron variant C/G;T snv 11
rs745826707 0.851 0.200 2 178112712 missense variant G/A;T snv 8.0E-06; 4.0E-06 5
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs8878 0.827 0.280 4 76021147 3 prime UTR variant A/C;G snv 5
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs9268645 0.827 0.360 6 32440750 intron variant C/G;T snv 5
rs9276291 0.925 0.200 6 32735036 upstream gene variant T/A;C snv 2
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23