ClinVar Miner

Submissions for variant NM_030662.4(MAP2K2):c.450+9G>T

dbSNP: rs375368051
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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 RCV002076711 SCV002330880 likely benign RASopathy 2021-08-17 criteria provided, single submitter clinical testing

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