Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12466865 2 64655280 intron variant C/T snv 0.30 2
rs140625215 2 64632896 3 prime UTR variant TTCAAA/- delins 0.26 2
rs6753848 2 64723661 intron variant C/G;T snv 2
rs12471768 2 64701469 intron variant T/C;G snv 1
rs2160348 2 64682032 intron variant T/C snv 0.68 1
rs3755189 2 64654863 intron variant G/A snv 0.35 1