ClinVar Miner

Submissions for variant NM_006258.4(PRKG1):c.1174-84G>T

dbSNP: rs10454466
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
GeneDx RCV001725051 SCV001950836 benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001725051 SCV005322641 benign not provided criteria provided, single submitter not provided

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