ClinVar Miner

Submissions for variant NM_001083961.2(WDR62):c.3763G>A (p.Val1255Ile)

gnomAD frequency: 0.00075  dbSNP: rs146180208
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000416274 SCV000493535 uncertain significance not provided 2016-07-01 criteria provided, single submitter clinical testing
GeneDx RCV000416274 SCV000731153 likely benign not provided 2021-06-20 criteria provided, single submitter clinical testing
Invitae RCV000416274 SCV001085428 likely benign not provided 2023-10-29 criteria provided, single submitter clinical testing

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