ClinVar Miner

Submissions for variant NM_001385079.1(PDE10A):c.1692G>A (p.Ala564=)

dbSNP: rs220740
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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 RCV001509841 SCV001716737 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001788553 SCV002029475 benign Infantile-onset generalized dyskinesia with orofacial involvement 2021-09-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001788554 SCV002029476 benign Striatal degeneration, autosomal dominant 2 2021-09-05 criteria provided, single submitter clinical testing

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