ClinVar Miner

Submissions for variant NM_002524.5(NRAS):c.111+10A>G

dbSNP: rs1659156787
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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 RCV002147963 SCV002430387 likely benign RASopathy 2020-11-07 criteria provided, single submitter clinical testing

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