Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2874490 3 156917724 intron variant C/T snv 0.19 1
rs344081 3 156838195 intron variant T/C snv 0.24 1
rs74394007 3 156974418 intron variant A/C snv 0.17 1