ClinVar Miner

Submissions for variant NM_001164760.2(PRKAR1B):c.846T>C (p.Ile282=)

gnomAD frequency: 0.43881  dbSNP: rs3211362
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
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579376 SCV001806993 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001579376 SCV001966380 benign not specified no assertion criteria provided clinical testing

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