Submissions for variant NM_000548.5(TSC2):c.2220+1G>T (rs137854361)

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
Tuberous sclerosis database (TSC2)	RCV000043387	SCV000067193	not provided	Tuberous sclerosis syndrome		no assertion provided	curation
Baylor Genetics	RCV000722174	SCV000854627	pathogenic	Tuberous sclerosis 2	2018-11-18	no assertion criteria provided	clinical testing

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