ClinVar Miner

Submissions for variant NM_198525.3(KIF7):c.756C>T (p.Asp252=)

dbSNP: rs2142030504
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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 RCV002215258 SCV002364714 likely benign Acrocallosal syndrome 2023-09-25 criteria provided, single submitter clinical testing

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