Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs78487399 2 43582208 intron variant G/C snv 6.2E-02 5
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61