Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4927858 3 196045068 intron variant A/G snv 0.41 1
rs55649226 3 196076452 intron variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTTTTT delins 0.45 1
rs9859260 3 196073676 intron variant C/A;T snv 1