ClinVar Miner

Submissions for variant NM_001918.5(DBT):c.1281+31T>G

gnomAD frequency: 0.03046  dbSNP: rs115696850
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000079931 SCV000111814 benign not specified 2013-08-23 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV000079931 SCV000308530 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001555184 SCV001776556 likely benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003343634 SCV004050140 benign Maple syrup urine disease 2023-04-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001555184 SCV005258717 likely benign not provided criteria provided, single submitter not provided

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