ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.2112A>G (p.Pro704=) (rs926782023)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Integrated Genetics/Laboratory Corporation of America	RCV000590243	SCV000696885	likely benign	not specified	2019-08-28	criteria provided, single submitter	clinical testing

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