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 0.100 0.895 19 1998 2017
dbSNP: rs2070744
rs2070744
54 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.040 0.750 4 2013 2017
dbSNP: rs1800780
rs1800780
2 0.925 0.120 7 151001791 intron variant A/G snv 0.58 0.56 0.020 1.000 2 2013 2014
dbSNP: rs3918181
rs3918181
2 0.925 0.120 7 151004695 intron variant G/A snv 0.35 0.020 0.500 2 2013 2014
dbSNP: rs3918188
rs3918188
10 0.776 0.280 7 151005693 intron variant C/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs743506
rs743506
4 0.925 0.120 7 151009827 intron variant G/A;C snv 0.010 1.000 1 2016 2016