Variants with conflicting interpretations "likely pathogenic" from UCLA Clinical Genomics Center, UCLA and "benign" from any submitter

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001134831.2(AHI1):c.3257A>G (p.Glu1086Gly)	rs148000791	0.00115
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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