Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3131296 0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs9272535 0.827 0.280 6 32638979 synonymous variant G/A snv 3.0E-05 1.8E-03 5
rs9268856 0.807 0.240 6 32461942 intron variant C/A;T snv 4
rs9272219 0.925 0.160 6 32634492 intron variant G/T snv 0.29 4
rs3132935 0.925 0.160 6 32203298 non coding transcript exon variant A/G;T snv 2
rs9268862 0.925 0.160 6 32462390 intron variant A/C snv 0.29 2