Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs661171 11 110145794 intron variant T/G snv 0.69 5
rs10789752 11 110109220 intron variant T/A;C snv 1
rs689183 11 110141418 intron variant G/T snv 0.74 1
rs746463 11 110125219 intron variant C/T snv 0.71 1