Variants with conflicting interpretations "pathogenic" from SingHealth Duke-NUS Institute of Precision Medicine and "likely pathogenic" from any submitter

Minimum review status of the submission from SingHealth Duke-NUS Institute of Precision Medicine:		Collection method of the submission from SingHealth Duke-NUS Institute of Precision Medicine:
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_001370658.1(BTD):c.697C>T (p.Pro233Ser)	rs397514383	0.00001
NM_000053.4(ATP7B):c.1543+1G>T	rs1360279134
NM_000528.4(MAN2B1):c.2398G>C (p.Gly800Arg)	rs398123456

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