ClinVar Miner

Submissions for variant NM_005266.6(GJA5):c.-175G>A

gnomAD frequency: 0.19061  dbSNP: rs35594137
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000316019 SCV000482958 likely benign Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711024 SCV005261608 likely benign not provided criteria provided, single submitter not provided

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