ClinVar Miner

Submissions for variant NM_001184.4(ATR):c.1885+39T>C

gnomAD frequency: 0.10546  dbSNP: rs73240318
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
GeneDx RCV001594852 SCV001829045 benign not provided 2019-08-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001594852 SCV005303012 benign not provided criteria provided, single submitter not provided
Genetic Services Laboratory, University of Chicago RCV000145293 SCV000192370 likely benign not specified no assertion criteria provided clinical testing

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