ClinVar Miner

Submissions for variant NM_000103.4(CYP19A1):c.196C>T (p.Leu66=)

dbSNP: rs2033435368
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003574873 SCV004343383 likely benign not provided 2023-12-24 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279034 SCV001466090 uncertain significance Aromatase deficiency 2020-04-17 no assertion criteria provided clinical testing

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