Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs6214 0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs314277 0.925 0.080 6 104959787 intron variant A/C;G;T snv 6