ClinVar Miner

Submissions for variant NM_002734.5(PRKAR1A):c.892-34G>T

gnomAD frequency: 0.71288  dbSNP: rs2302231
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ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001685676 SCV001897262 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001789518 SCV002031846 benign Carney complex, type 1 2021-10-25 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001789519 SCV002031847 benign Acrodysostosis 1 with or without hormone resistance 2021-10-25 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001685676 SCV005255639 benign not provided criteria provided, single submitter not provided

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