Variants in gene combination SNHG14, UBE3A with conflicting interpretations reported as "benign and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_130839.5(UBE3A):c.2124+9T>C	rs79328837	0.00454
NM_130839.5(UBE3A):c.2618A>G (p.Ter873=)	rs76794400	0.00313
NM_130839.5(UBE3A):c.1269C>T (p.Asp423=)	rs149506027	0.00117
NM_130839.5(UBE3A):c.1767C>T (p.Tyr589=)	rs139082033	0.00096
NM_130839.5(UBE3A):c.927G>A (p.Ala309=)	rs576963061	0.00013
NM_130839.5(UBE3A):c.1338T>C (p.Phe446=)	rs371154816	0.00009
NM_130839.5(UBE3A):c.815A>G (p.Asn272Ser)	rs139928148	0.00009
NM_130839.5(UBE3A):c.1064G>C (p.Ser355Thr)	rs141984760	0.00004
NM_130839.5(UBE3A):c.592G>A (p.Ala198Thr)	rs147145506

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