ClinVar Miner

Submissions for variant NM_006031.6(PCNT):c.5994+13dup

dbSNP: rs772752236
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 RCV001817408 SCV002068174 uncertain significance not specified 2017-12-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002074283 SCV002342631 benign not provided 2024-02-12 criteria provided, single submitter clinical testing

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