ClinVar Miner

Submissions for variant NM_000046.5(ARSB):c.111G>C (p.Ser37=)

dbSNP: rs2112583225
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002207869 SCV002371938 likely benign Mucopolysaccharidosis type 6 2024-12-31 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002307836 SCV002600756 likely benign not specified 2022-10-28 criteria provided, single submitter clinical testing

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