Variants in gene CTNNB1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 6

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HGVS	dbSNP	gnomAD frequency
NM_001904.4(CTNNB1):c.2340C>T (p.Asp780=)	rs2293303	0.01246
NM_001904.4(CTNNB1):c.1983A>C (p.Arg661=)	rs1800663	0.00392
NM_001904.4(CTNNB1):c.2320C>T (p.Leu774=)	rs4135386	0.00390
NM_001904.4(CTNNB1):c.1023C>T (p.Ser341=)	rs34343353	0.00154
NM_001904.4(CTNNB1):c.860A>G (p.Asn287Ser)	rs35288908	0.00086
NM_001904.4(CTNNB1):c.1830C>T (p.Ile610=)	rs374923885	0.00023

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