Variants in gene PTEN with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000314.8(PTEN):c.-165C>G	rs575260016	0.00267
NM_000314.8(PTEN):c.-461G>A	rs1209261790	0.00114
NM_000314.8(PTEN):c.882T>G (p.Ser294Arg)	rs143335584	0.00029
NM_000314.8(PTEN):c.235G>A (p.Ala79Thr)	rs202004587	0.00011
NM_000314.8(PTEN):c.720C>T (p.Tyr240=)	rs190070312	0.00006
NM_000314.8(PTEN):c.1061C>A (p.Pro354Gln)	rs375709098	0.00003
NM_000314.8(PTEN):c.210-9T>C	rs751744545	0.00001
NM_000314.8(PTEN):c.78C>T (p.Thr26=)	rs786201280	0.00001
NM_000314.8(PTEN):c.*10dup	rs756681683
NM_000314.8(PTEN):c.-500GGC[7]	rs1237307954
NM_000314.8(PTEN):c.210-7_210-3del	rs587780544

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