ClinVar Miner

Submissions for variant NM_018368.4(LMBRD1):c.6G>A (p.Ala2=)

dbSNP: rs753043203
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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 RCV001430378 SCV001633110 likely benign Methylmalonic aciduria and homocystinuria type cblF 2022-01-15 criteria provided, single submitter clinical testing

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