ClinVar Miner

Submissions for variant NM_030662.4(MAP2K2):c.1116C>T (p.Ser372=)

dbSNP: rs772111297
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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 RCV002133158 SCV002445463 likely benign RASopathy 2023-06-19 criteria provided, single submitter clinical testing

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