ClinVar Miner

Submissions for variant NM_000182.5(HADHA):c.1621-26G>T

gnomAD frequency: 0.82473  dbSNP: rs1865324
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001527290 SCV001738252 benign Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency 2021-06-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004709067 SCV005244889 benign not provided criteria provided, single submitter not provided

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