Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9487023 6 109268801 intron variant A/G snv 0.40 8
rs11966072 6 109313625 intron variant A/G snv 0.26 4
rs13191948 6 109313396 intron variant C/T snv 0.40 2
rs9374080 6 109295217 intron variant T/C snv 0.40 1