Variants with conflicting interpretations "likely pathogenic" from UNC Molecular Genetics Laboratory, University of North Carolina at Chapel Hill and "pathogenic" from Ambry Genetics

Minimum review status of the submission from UNC Molecular Genetics Laboratory, University of North Carolina at Chapel Hill:		Collection method of the submission from UNC Molecular Genetics Laboratory, University of North Carolina at Chapel Hill:
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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP	gnomAD frequency
NM_001369.3(DNAH5):c.6249G>A (p.Met2083Ile)	rs753614861	0.00006
NM_012144.4(DNAI1):c.1212T>G (p.Tyr404Ter)	rs926347298	0.00004
NM_001369.3(DNAH5):c.10441C>T (p.Arg3481Ter)	rs886039500	0.00001
NM_001369.3(DNAH5):c.13458dup (p.Asn4487Ter)	rs775696136

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