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: rs1801394
rs1801394
101 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2011 2014
dbSNP: rs3776455
rs3776455
2 0.925 0.120 5 7896398 intron variant C/T snv 0.58 0.010 1.000 1 2013 2013