ClinVar Miner

Submissions for variant NM_000528.4(MAN2B1):c.1398G>A (p.Ala466=)

dbSNP: rs774396746
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000392764 SCV000410794 uncertain significance Deficiency of alpha-mannosidase 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000392764 SCV001595755 likely benign Deficiency of alpha-mannosidase 2024-01-25 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000392764 SCV002014541 likely benign Deficiency of alpha-mannosidase 2021-09-05 criteria provided, single submitter clinical testing

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