ClinVar Miner

Submissions for variant NM_005032.7(PLS3):c.582+8T>G

gnomAD frequency: 0.00086  dbSNP: rs189475474
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001579944 SCV002433101 benign not provided 2024-07-24 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579944 SCV001809127 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001579944 SCV001976181 likely benign not provided no assertion criteria provided clinical testing

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