Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1061808
rs1061808
2 6 32168770 3 prime UTR variant T/G snv 0.64 0.800 1.000 1 2012 2012
dbSNP: rs3134950
rs3134950
2 6 32159700 intron variant C/A snv 0.64 0.700 1.000 1 2013 2013