ClinVar Miner

Submissions for variant NM_021939.4(FKBP10):c.246-3dup

dbSNP: rs781920419
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001546828 SCV001766416 likely benign not provided 2018-06-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001546828 SCV002338604 benign not provided 2024-01-22 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003966170 SCV004784866 likely benign FKBP10-related disorder 2024-07-28 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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