ClinVar Miner

Submissions for variant NM_016203.3(PRKAG2):c.-560C>T

gnomAD frequency: 0.04777  dbSNP: rs117728810
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000352884 SCV000467730 likely benign Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV001795991 SCV000467731 likely benign Wolff-Parkinson-White pattern 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001653720 SCV001866189 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001653720 SCV005219873 likely benign not provided criteria provided, single submitter not provided

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