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: rs34777958
rs34777958
1 1.000 0.040 16 84176003 missense variant C/T snv 9.8E-03 1.1E-02 0.010 1.000 1 2013 2013