ClinVar Miner

Submissions for variant NM_138927.4(SON):c.4216C>G (p.Pro1406Ala)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002962471 SCV003286437 benign not provided 2023-10-13 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002962471 SCV004011359 likely benign not provided 2023-06-01 criteria provided, single submitter clinical testing SON: BP4

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