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
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1171614 0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79 7
rs1865760 0.925 0.120 6 25916751 synonymous variant C/T snv 0.42 0.34 5
rs6706968 0.925 0.120 2 120552693 non coding transcript exon variant A/C;G snv 3