Variants with conflicting interpretations "likely benign" from Genome Diagnostics Laboratory, The Hospital for Sick Children and "risk factor" from any submitter

Minimum review status of the submission from Genome Diagnostics Laboratory, The Hospital for Sick Children:		Collection method of the submission from Genome Diagnostics Laboratory, The Hospital for Sick Children:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 1

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HGVS	dbSNP	gnomAD frequency
NM_000361.3(THBD):c.127G>A (p.Ala43Thr)	rs1800576	0.00255

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