ClinVar Miner

Submissions for variant NM_006912.6(RIT1):c.164-18C>G

dbSNP: rs2102585269
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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 RCV003741956 SCV004436555 likely benign Noonan syndrome 8 2023-01-25 criteria provided, single submitter clinical testing

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