Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2912054 8 6743971 intron variant G/C;T snv 3
rs2911971 8 6750113 intron variant C/G;T snv 2
rs2936512 8 6741484 intron variant T/C snv 0.76 1