ClinVar Miner

Submissions for variant NM_021951.3(DMRT1):c.671A>G (p.Asn224Ser)

gnomAD frequency: 0.00108  dbSNP: rs140506267
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Reproductive Genetics, University of Münster RCV000845253 SCV000987211 uncertain significance Non-obstructive azoospermia 2020-06-07 criteria provided, single submitter research
CeGaT Center for Human Genetics Tuebingen RCV000235005 SCV001155587 likely benign not provided 2018-01-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000235005 SCV001732499 benign not provided 2024-01-02 criteria provided, single submitter clinical testing
OMIM RCV000235005 SCV000292373 uncertain significance not provided 2018-09-11 no assertion criteria provided literature only

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