Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1473247 1.000 0.040 5 159176563 intron variant T/C snv 0.41 2
rs10076782 5 159177955 intron variant G/A snv 0.41 1
rs55801554 5 159195524 intron variant C/A snv 0.25 1