ClinVar Miner

Submissions for variant NM_014140.4(SMARCAL1):c.2388T>C (p.Ala796=)

dbSNP: rs2106086500
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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 RCV002212007 SCV002353829 likely benign Schimke immuno-osseous dysplasia 2021-06-02 criteria provided, single submitter clinical testing

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