Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs10484554 0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs241447 0.827 0.280 6 32828974 missense variant T/C snv 0.31 0.26 11