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: rs1553585262
rs1553585262
CRYGC ; LOC100507443
1 1.000 0.040 2 208128304 frameshift variant -/C delins 0.700 1.000 2 2009 2017