Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 19
rs2297440 0.763 0.080 20 63680946 intron variant T/C snv 0.81 9
rs4809324 0.807 0.200 20 63686867 non coding transcript exon variant T/C snv 8.8E-02 4
rs6062302 0.882 0.040 20 63689615 synonymous variant T/C snv 0.74 0.81 1
rs115303435 1.000 0.040 20 63694806 missense variant G/A snv 3.2E-03 1.1E-03 1