ClinVar Miner

Submissions for variant NM_001148.6(ANK2):c.9163T>G (p.Phe3055Val)

gnomAD frequency: 0.00001  dbSNP: rs1158664416
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
AiLife Diagnostics, AiLife Diagnostics RCV002224595 SCV002502168 uncertain significance not provided 2022-03-01 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002487025 SCV002787681 uncertain significance Cardiac arrhythmia, ankyrin-B-related 2021-10-14 criteria provided, single submitter clinical testing

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