ClinVar Miner

Submissions for variant NM_000795.4(DRD2):c.939T>C (p.His313=)

gnomAD frequency: 0.58390  dbSNP: rs6275
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000242384 SCV000305536 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001513860 SCV001721550 benign Dystonic disorder 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001711663 SCV001941740 benign not provided 2018-07-23 criteria provided, single submitter clinical testing
Center for Forensic Mental Health, Chiba University RCV003633489 SCV004543739 benign Schizophrenia criteria provided, single submitter case-control
Breakthrough Genomics, Breakthrough Genomics RCV001711663 SCV005231660 benign not provided criteria provided, single submitter not provided

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