ClinVar Miner

Submissions for variant NM_000255.4(MMUT):c.912-138C>T

dbSNP: rs9395492
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Pars Genome Lab RCV001530465 SCV001745302 benign Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency 2021-06-19 criteria provided, single submitter clinical testing
GeneDx RCV001712963 SCV001945098 benign not provided 2018-06-29 criteria provided, single submitter clinical testing

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