ClinVar Miner

Submissions for variant NM_012431.3(SEMA3E):c.9C>A (p.Ser3=)

dbSNP: rs754589877
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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 RCV003604168 SCV004409734 likely benign CHARGE syndrome 2022-10-27 criteria provided, single submitter clinical testing

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