ClinVar Miner

Submissions for variant NM_198525.3(KIF7):c.2191+11G>A

gnomAD frequency: 0.00003  dbSNP: rs199753549
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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 RCV002081161 SCV002378649 likely benign Acrocallosal syndrome 2022-06-07 criteria provided, single submitter clinical testing

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