ClinVar Miner

Submissions for variant NM_000429.3(MAT1A):c.-73_-72insGAAAAA

dbSNP: rs145126070
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000290891 SCV000365381 likely benign Hepatic methionine adenosyltransferase deficiency 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001597050 SCV001830268 benign not provided 2021-05-16 criteria provided, single submitter clinical testing

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