ClinVar Miner

Submissions for variant NM_000551.4(VHL):c.463+43A>G

gnomAD frequency: 0.01217  dbSNP: rs34661876
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001648782 SCV001861911 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268546 SCV002552406 benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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