ClinVar Miner

Submissions for variant NM_000103.4(CYP19A1):c.859-6G>T

gnomAD frequency: 0.00002  dbSNP: rs756838912
Minimum review status: Collection method:
Minimum conflict level:
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 RCV001427542 SCV001630226 likely benign not provided 2023-11-06 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279026 SCV001466081 uncertain significance Aromatase deficiency 2020-04-17 no assertion criteria provided clinical testing

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