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: rs762704392
rs762704392
1 1.000 0.080 2 112836208 missense variant C/T snv 2.4E-05 2.1E-05 0.010 1.000 1 2011 2011