ClinVar Miner

Submissions for variant NM_007373.4(SHOC2):c.972+12A>G

dbSNP: rs913524232
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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 RCV002076111 SCV002429829 likely benign RASopathy 2023-11-06 criteria provided, single submitter clinical testing

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