ClinVar Miner

Submissions for variant NM_001876.4(CPT1A):c.771+31C>T

gnomAD frequency: 0.00345  dbSNP: rs114802513
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 RCV001552681 SCV001773417 likely benign not provided 2018-08-15 criteria provided, single submitter clinical testing

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