ClinVar Miner

Submissions for variant NM_006258.4(PRKG1):c.1545+17C>A

dbSNP: rs745349839
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Human Genetics, Inc, Center for Human Genetics, Inc RCV000660233 SCV000782236 likely benign Connective tissue disorder 2016-11-01 criteria provided, single submitter clinical testing

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