Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1878561 1.000 0.040 8 8234883 intron variant A/C snv 0.57 1
rs2945232 1.000 0.040 8 8240516 non coding transcript exon variant T/C snv 0.47 1
rs2980436 1.000 0.040 8 8234503 non coding transcript exon variant G/A snv 0.42 1