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: rs587777534
rs587777534
CTSC
3 0.882 0.160 11 88296207 missense variant C/G;T snv 1.6E-05; 4.0E-06 0.010 1.000 1 2006 2006