ClinVar Miner

Submissions for variant NM_001876.4(CPT1A):c.281+266G>A

gnomAD frequency: 0.10048  dbSNP: rs2278905
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001716306 SCV001939946 benign not provided 2019-04-16 criteria provided, single submitter clinical testing

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