ClinVar Miner

Submissions for variant NM_000321.2(RB1):c.2084T>G (p.Met695Arg) (rs727504122)

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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	RCV000153811	SCV000203391	uncertain significance	not provided	2014-04-01	criteria provided, single submitter	clinical testing

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