Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112332300 1.000 0.080 3 23588427 intron variant T/-;TT;TTT;TTTT delins 1
rs12633613 1.000 0.080 3 23349016 intron variant T/C snv 0.27 1
rs1496653 1.000 0.080 3 23413299 intron variant A/G snv 0.26 1
rs1845900 1.000 0.080 3 23413074 intron variant A/C;G snv 1
rs7612463 0.925 0.080 3 23294959 intron variant C/A;G snv 1