Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs9808753 0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs1494555 0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8