ClinVar Miner

Submissions for variant NM_002755.4(MAP2K1):c.960+14G>A

dbSNP: rs200963333
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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 RCV002103612 SCV002399489 likely benign RASopathy 2022-04-18 criteria provided, single submitter clinical testing

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