ClinVar Miner

Submissions for variant NM_198525.3(KIF7):c.2652C>T (p.Ile884=)

gnomAD frequency: 0.00001  dbSNP: rs750064265
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001406476 SCV001608431 likely benign Acrocallosal syndrome 2023-04-12 criteria provided, single submitter clinical testing

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