ClinVar Miner

Submissions for variant NM_018368.4(LMBRD1):c.88T>C (p.Trp30Arg)

dbSNP: rs1582168492
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City RCV000984986 SCV001132912 uncertain significance Methylmalonic aciduria and homocystinuria type cblF 2019-08-25 no assertion criteria provided clinical testing

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