"All of Us Research Program, National Institutes of Health"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2202570	NM_000548.5(TSC2):c.-33_-30+10del	LOC130058210, TSC2	Deletion (splice donor variant)	Tuberous sclerosis syndrome +1 more	GUncertain significance
Select item 3070132	NM_000548.5(TSC2):c.-30_-30+11del	LOC130058210, TSC2	Deletion (splice donor variant)	Tuberous sclerosis syndrome	GUncertain significance
Select item 133423	NM_000548.5(TSC2):c.-30+1G>T	LOC130058210, TSC2	Single nucleotide variant (splice donor variant)	not provided +3 more	GUncertain significance

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