GPC3, glypican 3, 2719

N. diseases: 311; N. variants: 16
Disease: Neonatal hypoglycemia ×
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: rs886039908
rs886039908 		0.925 0.360 X 133536175 frameshift variant A/- delins
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.700 0