Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9569206 13 55129083 intron variant A/G snv 0.39 1
rs12875339 13 55147898 intron variant A/C;T snv 1
rs3120852 13 55149941 intron variant A/G;T snv 1