Variants with conflicting interpretations "uncertain significance" from Institute of Human Genetics, Cologne University and "benign" from any submitter

Minimum review status of the submission from Institute of Human Genetics, Cologne University:		Collection method of the submission from Institute of Human Genetics, Cologne University:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001378183.1(PIEZO2):c.3730G>A (p.Val1244Met)	rs73946020	0.00599
NM_001394062.1(MACF1):c.4045C>A (p.Leu1349Met)	rs141025026	0.00088
NM_001394062.1(MACF1):c.13379A>G (p.Asn4460Ser)	rs761190322

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