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 0.020 1.000 2 2009 2014
dbSNP: rs753482
rs753482
3 0.925 0.040 7 151009295 intron variant C/A;G;T snv 0.83; 4.0E-05; 3.1E-05; 4.4E-06 0.010 1.000 1 2014 2014