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: rs1801157
rs1801157
46 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 0.060 1.000 6 2009 2017
dbSNP: rs902016090
rs902016090
2 0.925 0.080 10 44377773 missense variant G/C snv 0.010 1.000 1 2013 2013