ClinVar Miner

Submissions for variant NM_020987.5(ANK3):c.2614+6del

dbSNP: rs370950407
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001172460 SCV000150252 likely benign not specified 2019-03-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000116331 SCV001103620 benign not provided 2023-12-21 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000116331 SCV004125448 benign not provided 2023-05-01 criteria provided, single submitter clinical testing ANK3: BP4, BS1, BS2

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