ClinVar Miner

Submissions for variant NM_015404.4(WHRN):c.1473C>T (p.Phe491=)

gnomAD frequency: 0.00003  dbSNP: rs886044241
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000294957 SCV000344112 uncertain significance not provided 2016-08-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000294957 SCV002453105 likely benign not provided 2024-10-07 criteria provided, single submitter clinical testing

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