Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6795735 0.882 0.120 3 64719689 intron variant C/A;G;T snv 6
rs111558778 1.000 0.080 3 64763995 intron variant G/A snv 7.0E-06 1
rs4607103 0.882 0.120 3 64726228 intron variant C/T snv 0.28 1
rs4611812 1.000 0.080 3 64713769 intron variant C/A;T snv 0.53 1