ClinVar Miner

Submissions for variant NM_001555.5(IGSF1):c.498G>C (p.Glu166Asp)

dbSNP: rs201255931
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001573896 SCV001800419 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001573896 SCV001924674 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001703017 SCV001927516 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001573896 SCV001966602 likely benign not provided no assertion criteria provided clinical testing

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