ClinVar Miner

Submissions for variant NM_000551.4(VHL):c.341-38C>T

gnomAD frequency: 0.00084  dbSNP: rs185858030
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 RCV001592665 SCV001823190 likely benign not provided 2018-07-10 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002465892 SCV002760271 benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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