ClinVar Miner

Submissions for variant NM_006031.6(PCNT):c.640-8T>G

dbSNP: rs587784314
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
Genetic Services Laboratory, University of Chicago RCV000147166 SCV000194532 benign not specified 2013-02-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003764893 SCV004628987 likely benign not provided 2023-12-09 criteria provided, single submitter clinical testing

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