ClinVar Miner

Submissions for variant NM_198525.3(KIF7):c.1299C>A (p.Pro433=)

dbSNP: rs921943205
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001452874 SCV001656551 likely benign Acrocallosal syndrome 2023-11-27 criteria provided, single submitter clinical testing
GeneDx RCV001577887 SCV001805365 likely benign not provided 2019-10-04 criteria provided, single submitter clinical testing

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