ClinVar Miner

Submissions for variant NM_198525.3(KIF7):c.2719-28CCCT[5]

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
GeneDx RCV001704592 SCV000565826 likely benign not provided 2019-05-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001467088 SCV001671106 likely benign Acrocallosal syndrome 2024-01-25 criteria provided, single submitter clinical testing

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