Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs3829251 0.851 0.120 11 71483513 intron variant G/A snv 0.21 8