ClinVar Miner

Submissions for variant NM_015275.3(WASHC4):c.2162G>A (p.Arg721His)

gnomAD frequency: 0.00268  dbSNP: rs74426960
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000504057 SCV000595335 uncertain significance not specified 2017-01-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000962277 SCV001109353 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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