Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs8283 0.882 0.120 6 32115523 3 prime UTR variant A/G snv 0.25 4
rs1150754 0.851 0.200 6 32082981 intron variant C/A;T snv 2
rs1150753 0.925 0.120 6 32092090 intron variant A/G snv 6.3E-02 1
rs3130342 1.000 0.080 6 32112369 non coding transcript exon variant A/C;G;T snv 1