ClinVar Miner

Submissions for variant NM_000528.4(MAN2B1):c.2619G>C (p.Pro873=)

dbSNP: rs372896479
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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 RCV001503928 SCV001708789 likely benign Deficiency of alpha-mannosidase 2024-01-09 criteria provided, single submitter clinical testing

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