Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3103267 2 232123872 intron variant A/C snv 0.72 1
rs6717918 2 232290400 intron variant T/C snv 0.42 1
rs7571816 2 232212354 intron variant A/G snv 7.4E-02 1