ClinVar Miner

Submissions for variant NM_001128205.2(SULF1):c.1111A>G (p.Ile371Val)

gnomAD frequency: 0.00410  dbSNP: rs118056333
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000591775 SCV000706162 benign not specified 2017-02-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000962920 SCV001110032 likely benign not provided 2025-01-25 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000962920 SCV005221631 likely benign not provided criteria provided, single submitter not provided
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000962920 SCV001740765 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000962920 SCV001965745 likely benign not provided no assertion criteria provided clinical testing

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