ClinVar Miner

Submissions for variant NM_198525.3(KIF7):c.1758A>G (p.Gly586=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003844618 SCV004648805 likely benign Acrocallosal syndrome 2022-12-05 criteria provided, single submitter clinical testing

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