Variants with conflicting interpretations "benign" from Athena Diagnostics and "protective" from any submitter

Minimum review status of the submission from Athena Diagnostics:		Collection method of the submission from Athena Diagnostics:
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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000744.7(CHRNA4):c.1659G>A (p.Ala553=)	rs1044397	0.40553
NM_000744.7(CHRNA4):c.1629C>T (p.Ser543=)	rs1044396	0.40465

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