Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs34290285 0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs16903574 0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs3785356 0.925 0.080 16 27337847 intron variant C/T snv 0.25 5
rs55646091 0.925 0.080 11 76588387 upstream gene variant G/A snv 3.0E-02 5
rs705699 0.882 0.160 12 55991020 non coding transcript exon variant G/A snv 0.40 5
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs11071559 0.925 0.080 15 60777789 intron variant C/T snv 0.23 4
rs12722502 0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs61894547 0.882 0.160 11 76537586 intron variant C/T snv 3.1E-02 4
rs12952581 0.925 0.080 17 49370984 intron variant G/A snv 0.42 0.28 3
rs13416555 1.000 0.080 2 8301605 intron variant C/A;G snv 3
rs7894791 1.000 0.080 10 8549406 intergenic variant C/A snv 0.36 2