ClinVar Miner

Submissions for variant NM_000392.5(ABCC2):c.958A>G (p.Met320Val) (rs375385616)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics	RCV000594270	SCV000708812	uncertain significance	not provided	2017-05-26	criteria provided, single submitter	clinical testing

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