Variants in gene PTEN with conflicting interpretations "pathogenic" and "likely benign"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000314.8(PTEN):c.235G>A (p.Ala79Thr)	rs202004587	0.00011
NM_000314.8(PTEN):c.79+7A>G	rs374331677	0.00001
NM_000314.8(PTEN):c.210-7_210-3del	rs587780544

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