ClinVar Miner

Submissions for variant NC_000012.12:g.80425096A>G

gnomAD frequency: 0.70860  dbSNP: rs10746164
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
Breakthrough Genomics, Breakthrough Genomics RCV004707647 SCV005231949 benign not provided criteria provided, single submitter not provided
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001528271 SCV001739721 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001528271 SCV001951367 benign not specified no assertion criteria provided clinical testing

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