Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17145750 0.925 0.120 7 73612048 intron variant C/A;T snv 7
rs1051921 0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs7800944 0.882 0.160 7 73621527 intron variant T/C snv 0.28 4
rs3812316 0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02 2
rs12531645 7 73609551 non coding transcript exon variant G/A;T snv 1