ClinVar Miner

Submissions for variant NM_002755.4(MAP2K1):c.694-19C>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002921987 SCV003258710 likely benign RASopathy 2022-05-21 criteria provided, single submitter clinical testing

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