Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs3099844 0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 13
rs74790047 0.851 0.120 12 6601978 missense variant A/C;G snv 2.0E-05; 1.2E-04; 5.2E-03 1.7E-03 7