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: rs1042636
rs1042636
23 0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 0.010 < 0.001 1 2007 2007
dbSNP: rs1801725
rs1801725
39 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 < 0.001 1 2007 2007
dbSNP: rs1801726
rs1801726
13 0.732 0.280 3 122284985 missense variant G/C snv 0.95 0.92 0.010 < 0.001 1 2007 2007
dbSNP: rs756322971
rs756322971
9 0.763 0.240 3 122284955 missense variant C/A;G snv 0.010 < 0.001 1 2007 2007