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
rs185819 0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 8
rs2269426 0.807 0.280 6 32108722 intron variant G/A snv 0.35 8
rs1150752 0.882 0.240 6 32096949 missense variant T/C;G snv 5.9E-02 3
rs3134954 0.882 0.240 6 32104116 intron variant C/T snv 0.90 3
rs1150754 0.851 0.200 6 32082981 intron variant C/A;T snv 2