ClinVar Miner

Submissions for variant NM_152419.3(HGSNAT):c.371+9C>T

dbSNP: rs1180753142
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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 RCV002201727 SCV002494999 likely benign Mucopolysaccharidosis, MPS-III-C; Retinitis pigmentosa 73 2024-04-06 criteria provided, single submitter clinical testing

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