Variants with conflicting interpretations "likely pathogenic" from Institute for Genomic Medicine, Nationwide Children's Hospital and "benign" from any submitter

Minimum review status of the submission from Institute for Genomic Medicine, Nationwide Children's Hospital:		Collection method of the submission from Institute for Genomic Medicine, Nationwide Children's Hospital:
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_000053.4(ATP7B):c.3045G>A (p.Leu1015=)	rs1801248	0.02598
NM_000275.3(OCA2):c.1441G>A (p.Ala481Thr)	rs74653330	0.00630

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