Variants with conflicting interpretations "likely benign" from Baylor Genetics and "pathogenic" from any submitter

Minimum review status of the submission from Baylor Genetics:		Collection method of the submission from Baylor Genetics:
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_001363.5(DKC1):c.-142C>G	rs199422241	0.00227
NM_201631.4(TGM5):c.1335G>C (p.Lys445Asn)	rs606231276	0.00003

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