ClinVar Miner

Submissions for variant NM_000528.4(MAN2B1):c.605G>C (p.Arg202Pro)

dbSNP: rs864621979
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV000207009 SCV002775363 uncertain significance Deficiency of alpha-mannosidase 2021-11-08 criteria provided, single submitter clinical testing
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000207009 SCV000243963 uncertain significance Deficiency of alpha-mannosidase 2012-06-07 no assertion criteria provided literature only

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