ClinVar Miner

Submissions for variant NM_000103.4(CYP19A1):c.907A>G (p.Met303Val)

gnomAD frequency: 0.00001  dbSNP: rs2031445857
Minimum review status: Collection method:
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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
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004699261 SCV005205160 uncertain significance not specified 2024-06-17 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279025 SCV001466080 uncertain significance Aromatase deficiency 2020-04-17 no assertion criteria provided clinical testing

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