ClinVar Miner

Submissions for variant NM_001148.6(ANK2):c.10431C>A (p.Phe3477Leu)

dbSNP: rs2154031171
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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 RCV002224186 SCV002501883 uncertain significance not provided 2021-08-10 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002496152 SCV002791432 uncertain significance Cardiac arrhythmia, ankyrin-B-related 2021-07-05 criteria provided, single submitter clinical testing

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