ClinVar Miner

Submissions for variant NM_198525.3(KIF7):c.3954T>C (p.Phe1318=)

dbSNP: rs2141991003
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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 RCV002190912 SCV002482008 likely benign Acrocallosal syndrome 2020-12-21 criteria provided, single submitter clinical testing

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