ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.1098T>G (p.Ser366=)

dbSNP: rs2132465936
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702984 SCV001929769 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001702984 SCV001971869 likely benign not provided no assertion criteria provided clinical testing

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