ClinVar Miner

Submissions for variant NM_000103.4(CYP19A1):c.451+8G>A

gnomAD frequency: 0.00118  dbSNP: rs28892004
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 RCV000922933 SCV001068382 benign not provided 2024-09-26 criteria provided, single submitter clinical testing
Natera, Inc. RCV001273379 SCV001456386 benign Aromatase deficiency 2020-09-16 no assertion criteria provided clinical testing

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