ClinVar Miner

Submissions for variant NM_005266.7(GJA5):c.-67G>A

gnomAD frequency: 0.00108  dbSNP: rs36214923
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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 RCV000387823 SCV000348127 uncertain significance Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002275008 SCV002562937 benign not provided 2022-07-01 criteria provided, single submitter clinical testing GJA5: BS1, BS2
Breakthrough Genomics, Breakthrough Genomics RCV002275008 SCV005186879 uncertain significance not provided criteria provided, single submitter not provided

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