ClinVar Miner

Submissions for variant NM_020547.3(AMHR2):c.622-6C>T

gnomAD frequency: 0.16377  dbSNP: rs2071558
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000625000 SCV000743471 benign Persistent Mullerian duct syndrome 2016-11-16 criteria provided, single submitter clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000625000 SCV000744723 benign Persistent Mullerian duct syndrome 2017-05-31 criteria provided, single submitter clinical testing
GeneDx RCV001644711 SCV001859152 benign not provided 2019-03-12 criteria provided, single submitter clinical testing
Invitae RCV001644711 SCV002377811 benign not provided 2024-01-29 criteria provided, single submitter clinical testing

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