ClinVar Miner

Submissions for variant NM_198525.3(KIF7):c.329-14C>T

gnomAD frequency: 0.00004  dbSNP: rs1013318465
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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 RCV002090734 SCV002379008 likely benign Acrocallosal syndrome 2022-12-31 criteria provided, single submitter clinical testing

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