ClinVar Miner

Submissions for variant NM_001609.4(ACADSB):c.*3736G>T

gnomAD frequency: 0.00018  dbSNP: rs80159677
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV001103241 SCV001259974 benign Deficiency of 2-methylbutyryl-CoA dehydrogenase 2017-04-27 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases was too high to be consistent with this variant causing disease. Therefore, this variant is classified as benign.

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