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: rs45567233
rs45567233
CTSG
3 0.882 0.200 14 24574465 missense variant T/C snv 8.0E-02 5.9E-02 0.010 1.000 1 2001 2001