ClinVar Miner

Submissions for variant NM_198334.3(GANAB):c.996+21A>G

gnomAD frequency: 0.30391  dbSNP: rs10897289
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 RCV001647751 SCV001857128 benign not provided 2019-07-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001647751 SCV005316713 benign not provided criteria provided, single submitter not provided

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