Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10197031 2 104838132 intron variant T/A;C snv 1
rs1451533 2 104849547 intron variant G/A snv 0.28 1
rs6739199 2 104835868 intron variant C/G;T snv 1