CRYGC, crystallin gamma C, 1420

N. diseases: 60; N. variants: 13
Disease: Embryonal nuclear cataract (disorder) ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137853924
rs137853924 		0.851 0.200 2 208128343 missense variant C/A;T snv
CUI: C0158551
Disease: Embryonal nuclear cataract (disorder)
Embryonal nuclear cataract (disorder) 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.020 1.000 2 2012 2015