ClinVar Miner

Submissions for variant NM_001876.4(CPT1A):c.2235+178A>G

gnomAD frequency: 0.01070  dbSNP: rs111558940
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002251651 SCV002522063 likely benign not provided 2021-05-24 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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