ClinVar Miner

Submissions for variant NM_183050.4(BCKDHB):c.84C>G (p.Gly28=)

dbSNP: rs776261412
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002097337 SCV002387492 likely benign Maple syrup urine disease 2022-09-18 criteria provided, single submitter clinical testing

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