ClinVar Miner

Submissions for variant NM_014049.5(ACAD9):c.632A>G (p.Lys211Arg)

dbSNP: rs1257611357
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Kids Research, The Children's Hospital at Westmead RCV001089483 SCV001244716 likely pathogenic Acyl-CoA dehydrogenase 9 deficiency criteria provided, single submitter research

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