ClinVar Miner

Submissions for variant NM_001918.5(DBT):c.1150= (p.Ser384=)

gnomAD frequency: 0.12900  dbSNP: rs12021720
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000532824 SCV000627806 benign Maple syrup urine disease 2024-02-01 criteria provided, single submitter clinical testing
OMIM RCV003581563 SCV000032962 pathogenic Maple syrup urine disease type 2 1998-01-01 no assertion criteria provided literature only
SingHealth Duke-NUS Institute of Precision Medicine RCV000532824 SCV000853182 benign Maple syrup urine disease 2017-06-07 no assertion criteria provided curation

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