ClinVar Miner

Submissions for variant NM_000103.4(CYP19A1):c.146-5C>T

dbSNP: rs2033440025
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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 RCV001413342 SCV001615454 likely benign not provided 2020-02-11 criteria provided, single submitter clinical testing

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