Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7225002 0.925 0.080 17 46111701 intron variant A/G snv 0.39 7
rs8067056 0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 5
rs199505 0.925 0.120 17 46782044 intron variant A/G snv 0.84 4
rs754593 1.000 0.040 17 45977330 non coding transcript exon variant G/A snv 0.52 4
rs2435200 0.925 0.080 17 45994485 intron variant G/A snv 0.40 3