ClinVar Miner

Submissions for variant NM_001184.4(ATR):c.4852+21C>T

dbSNP: rs587783332
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 RCV001657831 SCV001873281 benign not provided 2018-07-13 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000145317 SCV000192394 likely benign not specified no assertion criteria provided clinical testing

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