Variants with conflicting interpretations "pathogenic" from MedGen Diagnostic Laboratory, MedGen Medical Centre and "likely pathogenic" from any submitter

Minimum review status of the submission from MedGen Diagnostic Laboratory, MedGen Medical Centre:		Collection method of the submission from MedGen Diagnostic Laboratory, MedGen Medical Centre:
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_000049.4(ASPA):c.744+1G>A	rs2073877472
NM_003718.5(CDK13):c.484dup (p.Ala162fs)	rs1405252481

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