ClinVar Miner

Variants with conflicting interpretations "pathogenic" from GenMed Metabolism Lab and "uncertain significance" from Eurofins NTD LLC (GA)

Minimum review status of the submission from GenMed Metabolism Lab:		Collection method of the submission from GenMed Metabolism Lab:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
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Total variants with conflicting interpretations: 1

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HGVS	dbSNP	gnomAD frequency
NM_000531.6(OTC):c.572T>G (p.Leu191Arg)	rs72556297

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