ClinVar Miner

Submissions for variant NM_000103.4(CYP19A1):c.1215G>A (p.Glu405=)

dbSNP: rs772960231
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002172181 SCV002333740 likely benign not provided 2021-03-23 criteria provided, single submitter clinical testing

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