ClinVar Miner

Submissions for variant NM_002755.4(MAP2K1):c.420T>C (p.Ser140=)

dbSNP: rs2140584315
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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 RCV001441820 SCV001644759 likely benign RASopathy 2019-02-04 criteria provided, single submitter clinical testing

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