ClinVar Miner

Submissions for variant NM_198525.3(KIF7):c.2484G>C (p.Val828=)

dbSNP: rs774738288
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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 RCV001493337 SCV001697960 likely benign Acrocallosal syndrome 2022-10-14 criteria provided, single submitter clinical testing

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