ClinVar Miner

Submissions for variant NM_000795.4(DRD2):c.811-83G>T

gnomAD frequency: 0.15827  dbSNP: rs1076560
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000630731 SCV000751698 benign Dystonic disorder 2024-01-22 criteria provided, single submitter clinical testing
GeneDx RCV001662373 SCV001872409 benign not provided 2021-06-18 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 17196743, 22569179, 18077373, 21150907, 26347318, 19940176, 18829695)

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