ClinVar Miner

Submissions for variant NM_002755.4(MAP2K1):c.961-10G>C

dbSNP: rs2140682882
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001475448 SCV001679638 likely benign RASopathy 2024-10-04 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005005938 SCV005630956 uncertain significance Melorheostosis; Cardiofaciocutaneous syndrome 3 2024-03-10 criteria provided, single submitter clinical testing

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