ClinVar Miner

Submissions for variant NM_000018.4(ACADVL):c.62+6T>C

dbSNP: rs1555527495
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000498130 SCV000589747 likely pathogenic not provided 2016-02-26 criteria provided, single submitter clinical testing
Counsyl RCV000664668 SCV000788669 uncertain significance Very long chain acyl-CoA dehydrogenase deficiency 2018-01-13 no assertion criteria provided clinical testing

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