ClinVar Miner

Submissions for variant NM_198525.3(KIF7):c.1422G>A (p.Ala474=)

dbSNP: rs781285831
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000907384 SCV001986943 likely benign not provided 2021-04-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002065757 SCV002440222 likely benign Acrocallosal syndrome 2021-11-19 criteria provided, single submitter clinical testing

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