Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4775301 0.925 0.040 15 60834660 intron variant T/C;G snv 2
rs8024133 0.925 0.040 15 60838440 intron variant C/T snv 0.42 2
rs8041061 0.925 0.040 15 60832639 intron variant G/T snv 0.39 2
rs8042149 0.882 0.160 15 60832754 intron variant T/G snv 0.44 2