Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2076530 0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 5
rs2395182 0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76 5
rs3817963 0.776 0.360 6 32400310 intron variant T/C snv 0.25 5
rs615672 0.851 0.240 6 32606394 intergenic variant G/A;C snv 5
rs7194 0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 5
rs3129768 0.851 0.240 6 32627306 upstream gene variant G/T snv 0.76 4
rs9268402 0.827 0.200 6 32373576 intron variant G/A snv 0.45 4
rs3763307 0.882 0.200 6 32406845 non coding transcript exon variant A/T snv 0.24 3
rs9268403 0.807 0.240 6 32373696 intron variant T/C snv 0.24 3
rs9268480 0.882 0.200 6 32396067 synonymous variant C/T snv 0.26 0.24 3
rs9271640 0.925 0.120 6 32624423 upstream gene variant T/C snv 0.76 2