Variants in gene TSC1 with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_000368.5(TSC1):c.1029+3A>G	rs1554817334
NM_000368.5(TSC1):c.134T>C (p.Leu45Ser)	rs1554820662
NM_000368.5(TSC1):c.2042-5A>G	rs118203627
NM_000368.5(TSC1):c.2502+1G>T	rs2131702478
NM_000368.5(TSC1):c.350T>C (p.Leu117Pro)	rs118203368
NM_000368.5(TSC1):c.737+3A>G	rs118203439
NM_000368.5(TSC1):c.737G>T (p.Arg246Met)	rs118203436
Single allele

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