ClinVar Miner

Submissions for variant NM_138959.3(VANGL1):c.813-45C>A

gnomAD frequency: 0.64088  dbSNP: rs10754330
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001708459 SCV001934858 benign not provided 2021-06-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243436 SCV002514423 benign Sacral defect with anterior meningocele 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001708459 SCV005280489 benign not provided criteria provided, single submitter not provided

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