ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Athena Diagnostics Inc and "pathogenic" from Eurofins NTD LLC (GA)

Minimum review status of the submission from Athena Diagnostics Inc:		Collection method of the submission from Athena Diagnostics Inc:
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_182961.4(SYNE1):c.16390-2A>C	rs759460806
Single allele

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