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: rs1799983
rs1799983
246 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.030 1.000 3 2009 2015
dbSNP: rs1800780
rs1800780
2 0.925 0.120 7 151001791 intron variant A/G snv 0.58 0.56 0.010 1.000 1 2014 2014
dbSNP: rs3918181
rs3918181
2 0.925 0.120 7 151004695 intron variant G/A snv 0.35 0.010 1.000 1 2014 2014