ClinVar Miner

Submissions for variant NM_000103.4(CYP19A1):c.146-7G>T

gnomAD frequency: 0.00001  dbSNP: rs1262602894
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002541699 SCV003470666 likely benign not provided 2023-03-23 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279035 SCV001466091 uncertain significance Aromatase deficiency 2020-04-17 no assertion criteria provided clinical testing

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