ClinVar Miner

Submissions for variant NM_000479.5(AMH):c.864C>G (p.Asp288Glu)

dbSNP: rs199831511
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001443521 SCV001646496 likely benign not provided 2024-11-06 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003136078 SCV003826211 uncertain significance Persistent Mullerian duct syndrome 2020-09-16 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001443521 SCV003918032 likely benign not provided 2024-09-01 criteria provided, single submitter clinical testing AMH: BS1:Supporting, BS3:Supporting

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