Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10488140 1.000 0.040 7 55070695 intron variant C/T snv 0.26 1
rs17172438 1.000 0.040 7 55083844 intron variant T/C snv 0.21 1
rs729969 1.000 0.040 7 55060514 intron variant A/G;T snv 1