ClinVar Miner

Submissions for variant NM_001023.4(RPS20):c.4-90G>A

gnomAD frequency: 0.02357  dbSNP: rs73592343
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 RCV001640880 SCV001856563 benign not provided 2019-06-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001640880 SCV005266097 benign not provided criteria provided, single submitter not provided

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