List of variants in gene CTNNB1 reported as uncertain significance for retinal disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001904.4(CTNNB1):c.2140C>T (p.Pro714Ser)
NM_001904.4(CTNNB1):c.2181T>G (p.Asp727Glu)

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