Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs1307997067 0.851 0.320 17 3664199 missense variant A/C;G snv 4.0E-06 7.0E-06 7
rs8878 0.827 0.280 4 76021147 3 prime UTR variant A/C;G snv 5
rs3957148 0.925 0.160 6 32714360 upstream gene variant A/C;G snv 0.10 4
rs10770141 1.000 0.120 11 2172610 upstream gene variant A/C;G snv 2
rs241425 0.925 0.160 6 32837132 intron variant A/C;G snv 2
rs7679475 0.925 0.120 4 121392885 intergenic variant A/C;G snv 2
rs10011025 1.000 0.120 4 174733072 intron variant A/C;G snv 1
rs1805070 1.000 0.120 4 6301953 missense variant A/C;G snv 1.4E-04; 7.3E-03 1
rs1950942 1.000 0.120 14 105861856 upstream gene variant A/C;G snv 1
rs2286899 1.000 0.120 7 150743626 3 prime UTR variant A/C;G snv 1
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs11145763 0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs1805011 0.776 0.320 16 27362551 missense variant A/C;G;T snv 0.13; 1.2E-04; 3.6E-05 8
rs1800783 0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs1131580 0.882 0.160 3 172505830 3 prime UTR variant A/C;G;T snv 4
rs3134603 0.851 0.360 6 32158225 non coding transcript exon variant A/C;G;T snv 4
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs6476839 0.925 0.120 9 4290823 intron variant A/C;T snv 3
rs3094061 0.925 0.160 6 30353412 downstream gene variant A/C;T snv 2