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: rs4150167
rs4150167
1 1.000 0.040 16 84180078 missense variant C/T snv 1.9E-02 1.5E-02 0.800 1.000 1 2012 2012