List of variants in gene TSC2 reported as not provided for not provided

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000548.5(TSC2):c.1120-93T>C	rs17135764	0.56219
NM_000548.4(TSC2):c.1600_1716del (p.Val534_Gln572del)
NM_000548.5(TSC2):c.1119+2T>C	rs137854173
NM_000548.5(TSC2):c.1716+1G>T	rs45517190
NM_000548.5(TSC2):c.1946+2T>C	rs397515247
NM_000548.5(TSC2):c.3132-1G>C	rs45443096
NM_000548.5(TSC2):c.3285-3C>G	rs781023043
NM_000548.5(TSC2):c.3610+1G>C	rs45517299
NM_000548.5(TSC2):c.4889_4989+135del	rs137854272

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