ClinVar Miner

Submissions for variant NM_001008537.3(NEXMIF):c.3709A>T (p.Met1237Leu) (rs61731613)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000716507 SCV000847348 benign History of neurodevelopmental disorder 2014-09-30 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000712140 SCV000842563 likely benign not provided 2018-06-14 criteria provided, single submitter clinical testing
Invitae RCV000530431 SCV000653824 benign Mental retardation, X-linked 98 2018-01-10 criteria provided, single submitter clinical testing

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