Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9274299 1.000 0.040 6 32664181 non coding transcript exon variant C/A;G;T snv 1.7E-03 2
rs9274390 0.925 0.080 6 32664882 missense variant C/G;T snv 3.9E-02 2
rs9274657 1.000 0.040 6 32668587 upstream gene variant G/A snv 0.37 2
rs77296290 1.000 0.040 6 32667519 intron variant C/T snv 1
rs9274623 1.000 0.040 6 32668221 intron variant G/C;T snv 1