Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs143383 0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47 17