ClinVar Miner

Submissions for variant NM_000784.4(CYP27A1):c.453A>G (p.Gly151=)

dbSNP: rs2105979882
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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 RCV001438383 SCV001641255 likely benign Cholestanol storage disease 2020-04-08 criteria provided, single submitter clinical testing

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