Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs3764147 0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 4
rs6478108 0.763 0.200 9 114796423 intron variant C/T snv 0.73 3
rs10114470 0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 2
rs4574921 0.882 0.160 9 114776054 upstream gene variant C/T snv 0.80 2