Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs724577 4 17991787 intron variant A/C snv 0.71 2
rs16896068 4 17943217 intron variant G/A snv 0.25 1
rs2707450 4 17940937 intron variant C/T snv 0.73 1
rs2724475 4 17944809 intron variant T/C snv 0.71 1
rs6830062 4 18016107 intron variant T/C snv 0.25 1
rs6845078 4 17950585 intron variant C/A;T snv 1
rs7692995 4 17935011 intron variant T/C snv 0.23 1
rs925098 4 17918188 intron variant G/A snv 0.70 1