ClinVar Miner

Submissions for variant NM_005585.5(SMAD6):c.288A>G (p.Pro96=)

dbSNP: rs957321968
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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 RCV001429202 SCV001631916 likely benign Aortic valve disease 2 2018-03-08 criteria provided, single submitter clinical testing

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