Variants with conflicting interpretations "likely pathogenic" from UCLA Clinical Genomics Center, UCLA and "benign" from Labcorp Genetics (formerly Invitae), Labcorp

Minimum review status of the submission from UCLA Clinical Genomics Center, UCLA:		Collection method of the submission from UCLA Clinical Genomics Center, UCLA:
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_005921.2(MAP3K1):c.770C>T (p.Pro257Leu)	rs56160159	0.00001
NM_053025.4(MYLK):c.2149G>T (p.Asp717Tyr)	rs150936840

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