ClinVar Miner

Submissions for variant NM_198525.3(KIF7):c.2719-28CCCT[9]

dbSNP: rs3840030
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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 RCV001433597 SCV001636388 likely benign Acrocallosal syndrome 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV001555650 SCV001777099 likely benign not provided 2020-12-16 criteria provided, single submitter clinical testing Has not been previously published as pathogenic or benign to our knowledge

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