ClinVar Miner

Submissions for variant NM_198525.3(KIF7):c.1923-20C>A

gnomAD frequency: 0.00005  dbSNP: rs201211373
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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 RCV002160005 SCV002412210 likely benign Acrocallosal syndrome 2023-10-30 criteria provided, single submitter clinical testing

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