Variants with conflicting interpretations "likely pathogenic" from ClinVar Staff, National Center for Biotechnology Information (NCBI) and "benign" from any submitter

Minimum review status of the submission from ClinVar Staff, National Center for Biotechnology Information (NCBI):		Collection method of the submission from ClinVar Staff, National Center for Biotechnology Information (NCBI):
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_032578.4(MYPN):c.3335C>T (p.Pro1112Leu)	rs71534278	0.00318

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