Source: ALL
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: rs35953626
rs35953626
CRMP1 ; EVC
1 1.000 0.120 4 5753797 missense variant G/A snv 1.8E-02 7.1E-02 0.700 1.000 3 2000 2010