Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121917815 0.925 0.120 3 186854303 missense variant C/T snv 4.0E-06; 1.2E-05 2
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 1
rs2241767 0.763 0.440 3 186853407 intron variant A/G snv 0.10 1
rs17366568 0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02 1