ClinVar Miner

Submissions for variant NM_002734.5(PRKAR1A):c.*1244T>C

gnomAD frequency: 0.22809  dbSNP: rs9925
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000259768 SCV000405934 benign Carney complex 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000319592 SCV000405935 benign Acrodysostosis 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004710823 SCV005255643 benign not provided criteria provided, single submitter not provided

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