ClinVar Miner

Submissions for variant NM_016379.4(VCX3A):c.505C>G (p.Gln169Glu)

gnomAD frequency: 0.00109  dbSNP: rs137964452
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV001573235 SCV005207929 likely benign not provided criteria provided, single submitter not provided
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001573235 SCV001798791 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001727882 SCV001970997 benign not specified no assertion criteria provided clinical testing

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