Variants with conflicting interpretations "pathogenic" from University of Washington Center for Mendelian Genomics, University of Washington and "uncertain significance" from any submitter

Minimum review status of the submission from University of Washington Center for Mendelian Genomics, University of Washington:		Collection method of the submission from University of Washington Center for Mendelian Genomics, University of Washington:
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_018677.4(ACSS2):c.1487T>C (p.Val496Ala)	rs59088485	0.00096
NM_001009999.3(KDM1A):c.1739A>G (p.Asp580Gly)	rs864309716
NM_005787.6(ALG3):c.749T>A (p.Leu250Gln)	rs2108440795

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