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: rs12051350
rs12051350
1 1.000 0.120 16 18896946 missense variant C/T snv 3.7E-02 1.5E-02 0.010 1.000 1 2019 2019