Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs2285053 0.752 0.320 16 55478465 intron variant C/T snv 0.12 15
rs7201 0.925 0.160 16 55505702 3 prime UTR variant A/C snv 0.37 4
rs371828436 1.000 0.120 16 55489798 missense variant G/A;T snv 4.0E-06 1
rs780391868 1.000 0.120 16 55491915 missense variant G/A;C;T snv 8.0E-06 1