ClinVar Miner

Submissions for variant NM_015404.4(WHRN):c.1870C>T (p.Pro624Ser)

gnomAD frequency: 0.00105  dbSNP: rs140759343
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001585152 SCV001818477 likely benign not provided 2021-02-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001585152 SCV002443443 benign not provided 2023-12-09 criteria provided, single submitter clinical testing

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