ClinVar Miner

Submissions for variant NM_024411.5(PDYN):c.106G>T (p.Gly36Cys)

gnomAD frequency: 0.00067  dbSNP: rs149056587
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000517756 SCV000614430 benign not specified 2016-11-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000900279 SCV001044588 likely benign not provided 2023-06-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002490885 SCV002802612 likely benign Spinocerebellar ataxia type 23 2022-04-28 criteria provided, single submitter clinical testing

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