ClinVar Miner

Submissions for variant NM_001083961.2(WDR62):c.3336-5C>A

dbSNP: rs587784555
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001727093 SCV001961811 uncertain significance not provided 2021-07-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001727093 SCV005697059 likely benign not provided 2024-11-11 criteria provided, single submitter clinical testing

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