ClinVar Miner

Submissions for variant NM_001148.6(ANK2):c.11032+20TG[13]

dbSNP: rs34201791
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001652754 SCV001865939 benign not provided 2019-08-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073025 SCV002408919 benign Long QT syndrome 2024-02-01 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001652754 SCV003800224 benign not provided 2023-11-22 criteria provided, single submitter clinical testing

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