ClinVar Miner

Submissions for variant NM_001291088.2(WDR87):c.6901G>A (p.Glu2301Lys)

gnomAD frequency: 0.00576  dbSNP: rs565818371
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001769794 SCV002004710 likely benign not provided 2024-11-19 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Labcorp Genetics (formerly Invitae), Labcorp RCV001769794 SCV002474481 benign not provided 2024-01-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001769794 SCV005207071 likely benign not provided criteria provided, single submitter not provided

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