Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35928002 19 18005335 intron variant A/G snv 0.45 2
rs4808737 19 18006837 intron variant C/T snv 0.31 1
rs12981683 19 18003191 intron variant C/G;T snv 1
rs10411508 19 17999765 3 prime UTR variant G/A snv 0.35 1