ClinVar Miner

Submissions for variant NM_174916.3(UBR1):c.1282-42A>G

gnomAD frequency: 0.04765  dbSNP: rs2035169
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 RCV001690899 SCV001910069 benign not provided 2021-05-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001690899 SCV005290007 benign not provided criteria provided, single submitter not provided

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