List of variants in gene TSC2 reported as uncertain significance by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000548.5(TSC2):c.4569+12C>T	rs45517350	0.00008
NM_000548.5(TSC2):c.2294C>T (p.Ala765Val)	rs886042145	0.00002
NM_000548.5(TSC2):c.3397+15C>T	rs202246408	0.00001
NM_000548.5(TSC2):c.3212C>T (p.Thr1071Ile)	rs45498892

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