ClinVar Miner

Submissions for variant NM_000182.5(HADHA):c.573+26G>C

gnomAD frequency: 0.17547  dbSNP: rs35746418
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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 RCV001527293 SCV001738255 benign Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency 2021-06-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004710301 SCV005237888 benign not provided criteria provided, single submitter not provided

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