ClinVar Miner

Submissions for variant NM_000103.4(CYP19A1):c.903G>A (p.Leu301=)

dbSNP: rs2542401997
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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 RCV003553755 SCV004275121 likely benign not provided 2023-06-20 criteria provided, single submitter clinical testing

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