ClinVar Miner

Submissions for variant NM_001148.6(ANK2):c.11032+20TG[18]

dbSNP: rs34201791
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001638870 SCV001852275 benign not provided 2019-08-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002072957 SCV002407657 benign Long QT syndrome 2024-02-01 criteria provided, single submitter clinical testing

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