Submissions for variant NM_000548.5(TSC2):c.4663-38_4663-18dup (rs137854102)

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
GeneDx	RCV000189934	SCV000243601	benign	not specified	2015-01-14	criteria provided, single submitter	clinical testing	The variant is found in INFANT-EPI panel(s).
Tuberous sclerosis database (TSC2)	RCV000042573	SCV000066367	not provided	Tuberous sclerosis syndrome		no assertion provided	curation

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