Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs115829748 0.925 0.160 5 72098560 intron variant C/T snv 2.6E-02 2
rs143723948 0.925 0.160 9 37034098 5 prime UTR variant C/T snv 2
rs28641753 0.925 0.160 3 104256574 intergenic variant C/T snv 4.5E-02 2
rs73018809 0.925 0.160 3 13329174 intron variant A/T snv 2.0E-02 2