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: rs137853924
rs137853924
CRYGC ; LOC100507443
4 0.851 0.200 2 208128343 missense variant C/A;T snv 0.020 1.000 2 2012 2015