Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2253612 1.000 0.080 2 200703710 intron variant C/T snv 0.79 3
rs2540051 2 200706420 splice donor variant G/A snv 0.22 1
rs7563911 2 200711561 non coding transcript exon variant A/C;G;T snv 1
rs2348114 2 200717470 non coding transcript exon variant T/C snv 0.82 1
rs7589014 2 200716231 intron variant C/T snv 0.11 1