Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs12198173 0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs13199524 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 8
rs9368699 0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 7
rs2251396 0.827 0.240 6 31396930 upstream gene variant G/A snv 0.24 4