Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12670798 1.000 0.040 7 21567734 intron variant T/C snv 0.26 3
rs66476925 7 21571781 intron variant G/A;C;T snv 4.4E-06; 0.17; 4.4E-06 3
rs56130071 7 21559135 intron variant G/C snv 0.18 2
rs73066485 7 21572352 intron variant T/A;G snv 1