ClinVar Miner

Submissions for variant NM_139281.3(WDR36):c.1824G>A (p.Ser608=)

gnomAD frequency: 0.00016  dbSNP: rs189495008
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002938904 SCV003270651 benign not provided 2022-08-27 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002938904 SCV004159204 likely benign not provided 2023-03-01 criteria provided, single submitter clinical testing WDR36: BP4, BP7

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