Variants in gene SMARCB1 with conflicting interpretations "uncertain significance" and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (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: 2

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HGVS	dbSNP	gnomAD frequency
NM_003073.5(SMARCB1):c.110G>A (p.Arg37His)	rs398122368
NM_003073.5(SMARCB1):c.1120C>T (p.Arg374Trp)	rs1568963596

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