Submissions for variant NM_000314.7(PTEN):c.265C>T (p.Pro89Ser) (rs587783059)

Minimum review status:		Collection method:
Minimum conflict level:
		ClinVar version:

Total submissions: 2

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics	RCV000178755	SCV000230906	uncertain significance	not provided	2015-04-16	criteria provided, single submitter	clinical testing
Pathway Genomics	RCV000144659	SCV000189988	uncertain significance	Cowden syndrome 1	2014-07-24	no assertion criteria provided	clinical testing

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