Variants with conflicting interpretations "likely pathogenic" from Genome-Nilou Lab and "uncertain significance" from ClinVar Staff, National Center for Biotechnology Information (NCBI)

Minimum review status of the submission from Genome-Nilou Lab:		Collection method of the submission from Genome-Nilou Lab:
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_000528.4(MAN2B1):c.215A>T (p.His72Leu)	rs387906261
NM_000528.4(MAN2B1):c.2398G>C (p.Gly800Arg)	rs398123456

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