ClinVar Miner

Submissions for variant NM_000046.5(ARSB):c.723G>A (p.Val241=)

gnomAD frequency: 0.00001  dbSNP: rs199858121
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 RCV000930864 SCV001076522 likely benign Mucopolysaccharidosis type 6 2023-05-18 criteria provided, single submitter clinical testing
Natera, Inc. RCV000930864 SCV001458078 uncertain significance Mucopolysaccharidosis type 6 2020-01-24 no assertion criteria provided clinical testing

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